Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 50939 |
| ensemblid | ENSG00000081148.12 |
| hgncid | 18362 |
| symbol | IMPG2 |
| name | interphotoreceptor matrix proteoglycan 2 |
| refseq_nuc | NM_016247.4 |
| refseq_prot | NP_057331.2 |
| ensembl_nuc | ENST00000193391.8 |
| ensembl_prot | ENSP00000193391.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 101222546 |
| end | 101320575 |
| strand | - |
| ver | v1.2 |
| region | chr3:101222546-101320575 |
| region5000 | chr3:101217546-101325575 |
| regionname0 | IMPG2_chr3_101222546_101320575 |
| regionname5000 | IMPG2_chr3_101217546_101325575 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1241 | 215 | 53 | 37 | 95 | 8 | 22 | 77 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0002 | 1/1 | 1241 | 125 | 28 | 25 | 49 | 8 | 13 | 38 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0003 | 0/0 | 1241 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0004 | 0/0 | 1241 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0005 | 0/0 | 1241 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0006 | 0/0 | 1241 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0007 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0008 | 0/0 | 1241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0009 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0010 | 0/0 | 9 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(4): Show |
chr3 | 101217546 | 101325575 |
| a0011 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0012 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0013 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| a0014 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | MIMFP others(1236): Show |
chr3 | 101217546 | 101325575 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3723 | 214 | 53 | 37 | 94 | 8 | 22 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0001c0017 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0002c0002 | 1/1 | 3723 | 62 | 14 | 12 | 20 | 6 | 8 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0002c0003 | 0/0 | 3723 | 62 | 14 | 13 | 28 | 2 | 5 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0002c0013 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0003c0004 | 0/0 | 3723 | 4 | 4 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0003c0009 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0003c0014 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0004c0007 | 0/0 | 3723 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0005c0005 | 0/0 | 3723 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0006c0006 | 0/0 | 3723 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0007c0011 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0008c0015 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0009c0016 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0010c0008 | 0/0 | 3707 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3702): Show |
chr3 | 101217546 | 101325575 | ||
| a0011c0010 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0012c0018 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0013c0012 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 | ||
| a0014c0019 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | ATGAT others(3718): Show |
chr3 | 101217546 | 101325575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8314 | 89 | 21 | 14 | 42 | 4 | 8 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0006 | 0/0 | 8346 | 9 | 1 | 3 | 3 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8341): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0007 | 0/0 | 8356 | 9 | 2 | 0 | 7 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8351): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0008 | 0/0 | 8324 | 8 | 0 | 7 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8319): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0010 | 0/0 | 8360 | 7 | 1 | 1 | 3 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8355): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0012 | 0/0 | 8358 | 6 | 1 | 0 | 5 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8353): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0013 | 0/0 | 8362 | 6 | 0 | 0 | 4 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8357): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0014 | 0/0 | 8368 | 6 | 0 | 1 | 3 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8363): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0016 | 0/0 | 8366 | 5 | 0 | 0 | 5 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8361): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0020 | 0/0 | 8352 | 4 | 0 | 2 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0021 | 0/0 | 8364 | 3 | 1 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8359): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0022 | 0/0 | 8370 | 4 | 0 | 1 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8365): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0023 | 0/0 | 8316 | 3 | 0 | 0 | 1 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8311): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0025 | 0/0 | 8348 | 3 | 1 | 0 | 1 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0026 | 0/0 | 8352 | 3 | 3 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0029 | 0/0 | 8324 | 2 | 0 | 0 | 0 | 2 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8319): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0030 | 0/0 | 8314 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0031 | 0/0 | 8386 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8381): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0033 | 0/0 | 8344 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0034 | 0/0 | 8350 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8345): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0035 | 0/0 | 8350 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8345): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0036 | 0/0 | 8358 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8353): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0037 | 0/0 | 8362 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8357): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0038 | 0/0 | 8372 | 2 | 0 | 1 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8367): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0044 | 0/0 | 8314 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0051 | 0/0 | 8312 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8307): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0052 | 0/0 | 8312 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8307): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0053 | 0/0 | 8314 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0054 | 0/0 | 8314 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0055 | 0/0 | 8314 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0056 | 0/0 | 8314 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0060 | 0/0 | 8384 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8379): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0061 | 0/0 | 8336 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8331): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0062 | 0/0 | 8342 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8337): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0063 | 0/0 | 8342 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8337): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0064 | 0/0 | 8344 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0065 | 0/0 | 8344 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0066 | 0/0 | 8346 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8341): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0068 | 0/0 | 8348 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0069 | 0/0 | 8348 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0070 | 0/0 | 8352 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0071 | 0/0 | 8352 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0072 | 0/0 | 8352 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0073 | 0/0 | 8354 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8349): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0074 | 0/0 | 8358 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8353): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0077 | 0/0 | 8360 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8355): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0078 | 0/0 | 8362 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8357): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0079 | 0/0 | 8364 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8359): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0080 | 0/0 | 8364 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8359): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0081 | 0/0 | 8326 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8321): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0098 | 0/0 | 8353 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8348): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0099 | 0/0 | 8355 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8350): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0100 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8352): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0101 | 0/0 | 8363 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8358): Show |
chr3 | 101217546 | 101325575 |
| a0001c0001t0103 | 0/0 | 8314 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0001c0017t0001 | 0/0 | 8314 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0004 | 0/0 | 8348 | 7 | 1 | 0 | 5 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0009 | 0/0 | 8344 | 6 | 1 | 0 | 2 | 0 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0011 | 0/0 | 8342 | 7 | 0 | 3 | 1 | 2 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8337): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0015 | 0/0 | 8350 | 6 | 1 | 1 | 3 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8345): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0017 | 1/0 | 8352 | 4 | 0 | 0 | 1 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0027 | 0/0 | 8346 | 3 | 0 | 1 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8341): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0028 | 0/0 | 8360 | 3 | 0 | 1 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8355): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0039 | 0/0 | 8342 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8337): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0040 | 0/0 | 8340 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8335): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0041 | 0/0 | 8356 | 2 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8351): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0042 | 0/0 | 8358 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8353): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0043 | 0/0 | 8346 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8341): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0057 | 0/1 | 8298 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8293): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0082 | 0/0 | 8348 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0083 | 0/0 | 8320 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8315): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0084 | 0/0 | 8336 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8331): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0085 | 0/0 | 8338 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8333): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0086 | 0/0 | 8352 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0087 | 0/0 | 8360 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8355): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0088 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8363): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0089 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8365): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0090 | 0/0 | 8350 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8345): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0091 | 0/0 | 8310 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8305): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0092 | 0/0 | 8344 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0093 | 0/0 | 8354 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8349): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0094 | 0/0 | 8352 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0095 | 0/0 | 8362 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8357): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0096 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8363): Show |
chr3 | 101217546 | 101325575 |
| a0002c0002t0102 | 0/0 | 8345 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8340): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0002 | 0/0 | 8334 | 21 | 2 | 5 | 12 | 1 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8329): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0003 | 0/0 | 8336 | 16 | 1 | 2 | 9 | 1 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8331): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0005 | 0/0 | 8338 | 8 | 1 | 2 | 4 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8333): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0018 | 0/0 | 8320 | 5 | 4 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8315): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0019 | 0/0 | 8332 | 3 | 2 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8327): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0024 | 0/0 | 8340 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8335): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0032 | 0/0 | 8342 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8337): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0058 | 0/0 | 8332 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8327): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0059 | 0/0 | 8334 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8329): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0067 | 0/0 | 8348 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0075 | 0/0 | 8360 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8355): Show |
chr3 | 101217546 | 101325575 |
| a0002c0003t0097 | 0/0 | 8322 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8317): Show |
chr3 | 101217546 | 101325575 |
| a0002c0013t0019 | 0/0 | 8332 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8327): Show |
chr3 | 101217546 | 101325575 |
| a0003c0004t0046 | 0/0 | 8316 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8311): Show |
chr3 | 101217546 | 101325575 |
| a0003c0004t0047 | 0/0 | 8318 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8313): Show |
chr3 | 101217546 | 101325575 |
| a0003c0004t0048 | 0/0 | 8330 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8325): Show |
chr3 | 101217546 | 101325575 |
| a0003c0004t0049 | 0/0 | 8350 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8345): Show |
chr3 | 101217546 | 101325575 |
| a0003c0009t0050 | 0/0 | 8322 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8317): Show |
chr3 | 101217546 | 101325575 |
| a0003c0014t0045 | 0/0 | 8330 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8325): Show |
chr3 | 101217546 | 101325575 |
| a0004c0007t0001 | 0/0 | 8314 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0005c0005t0004 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0005c0005t0009 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0006c0006t0004 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0006c0006t0009 | 0/0 | 8344 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8339): Show |
chr3 | 101217546 | 101325575 |
| a0007c0011t0004 | 0/0 | 8348 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8343): Show |
chr3 | 101217546 | 101325575 |
| a0008c0015t0076 | 0/0 | 8360 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8355): Show |
chr3 | 101217546 | 101325575 |
| a0009c0016t0001 | 0/0 | 8314 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8309): Show |
chr3 | 101217546 | 101325575 |
| a0010c0008t0024 | 0/0 | 8324 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8319): Show |
chr3 | 101217546 | 101325575 |
| a0011c0010t0017 | 0/0 | 8352 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8347): Show |
chr3 | 101217546 | 101325575 |
| a0012c0018t0005 | 0/0 | 8338 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8333): Show |
chr3 | 101217546 | 101325575 |
| a0013c0012t0002 | 0/0 | 8334 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8329): Show |
chr3 | 101217546 | 101325575 |
| a0014c0019t0021 | 0/0 | 8364 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | AGAAA others(8359): Show |
chr3 | 101217546 | 101325575 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0002 | 0/0 | 6 | 1 | 1 | 3 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0012g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0014g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0016g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0020g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0021g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0021g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0022g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0023g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0023g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0023g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0025g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0025g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0025g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0026g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0026g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0026g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0029g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0029g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0030g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0030g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0031g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0033g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0033g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0034g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0034g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0035g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0035g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0036g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0036g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0037g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0037g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0038g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0038g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0044g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0051g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0052g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0053g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0054g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0055g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0056g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0060g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0061g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0062g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0063g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0064g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0065g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0066g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0068g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0069g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0070g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0071g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0072g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0073g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0074g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0077g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0078g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0079g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0080g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0081g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0098g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0099g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0100g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0101g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0001t0103g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0001c0017t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0009g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0011g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0015g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0017g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0027g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0027g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0027g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0028g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0028g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0028g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0039g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0039g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0040g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0040g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0041g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0041g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0042g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0042g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0043g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0057g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0082g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0083g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0084g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0085g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0086g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0087g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0088g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0089g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0090g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0091g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0092g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0093g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0094g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0095g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0096g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0002t0102g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0018g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0019g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0019g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0024g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0024g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0032g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0032g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0058g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0059g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0067g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0075g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0003t0097g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0002c0013t0019g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0046g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0047g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0048g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0004t0049g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0009t0050g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0003c0014t0045g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0004c0007t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0004c0007t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0005c0005t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0005c0005t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0006c0006t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0006c0006t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0007c0011t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0008c0015t0076g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0009c0016t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0010c0008t0024g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0011c0010t0017g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0012c0018t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0013c0012t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| a0014c0019t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00099 | hp2 | a0002 | c0002 | t0095 | g0072 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00140 | hp1 | a0002 | c0003 | t0003 | g0239 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00140 | hp2 | a0002 | c0002 | t0015 | g0294 | EUR | GBR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0123 | EUR | FIN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00280 | hp2 | a0002 | c0002 | t0011 | g0291 | EUR | FIN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0025 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00423 | hp1 | a0002 | c0003 | t0024 | g0268 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00423 | hp2 | a0007 | c0011 | t0004 | g0067 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00438 | hp1 | a0002 | c0002 | t0004 | g0220 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0144 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00597 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00621 | hp1 | a0001 | c0001 | t0022 | g0113 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00621 | hp2 | a0002 | c0002 | t0009 | g0079 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00639 | hp2 | a0002 | c0003 | t0075 | g0233 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00642 | hp2 | a0002 | c0002 | t0011 | g0009 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00673 | hp1 | a0002 | c0003 | t0002 | g0271 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0257 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00733 | hp2 | a0001 | c0001 | t0055 | g0049 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00735 | hp1 | a0002 | c0003 | t0002 | g0027 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00735 | hp2 | a0001 | c0001 | t0056 | g0172 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00741 | hp1 | a0002 | c0003 | t0067 | g0249 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0213 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0151 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01070 | hp2 | a0001 | c0001 | t0030 | g0056 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01071 | hp1 | a0002 | c0002 | t0011 | g0009 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01071 | hp2 | a0001 | c0001 | t0030 | g0058 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0139 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01081 | hp2 | a0002 | c0003 | t0002 | g0266 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01099 | hp1 | a0002 | c0002 | t0027 | g0293 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01106 | hp1 | a0002 | c0003 | t0019 | g0028 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01106 | hp2 | a0002 | c0002 | t0040 | g0300 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01167 | hp2 | a0002 | c0003 | t0005 | g0256 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01169 | hp1 | a0002 | c0003 | t0005 | g0254 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01169 | hp2 | a0002 | c0002 | t0028 | g0076 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01175 | hp2 | a0002 | c0002 | t0011 | g0301 | AMR | PUR | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01255 | hp1 | a0004 | c0007 | t0001 | g0206 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01255 | hp2 | a0002 | c0002 | t0040 | g0296 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01256 | hp2 | a0001 | c0001 | t0033 | g0158 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01258 | hp2 | a0001 | c0001 | t0033 | g0052 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01261 | hp2 | a0001 | c0001 | t0038 | g0127 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01358 | hp1 | a0004 | c0007 | t0001 | g0210 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0273 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01515 | hp2 | a0001 | c0001 | t0029 | g0103 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01516 | hp1 | a0002 | c0002 | t0017 | g0065 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01516 | hp2 | a0002 | c0002 | t0094 | g0295 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01517 | hp1 | a0002 | c0002 | t0011 | g0009 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01517 | hp2 | a0001 | c0001 | t0029 | g0102 | EUR | IBS | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01884 | hp1 | a0001 | c0001 | t0069 | g0149 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01891 | hp1 | a0003 | c0009 | t0050 | g0230 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01891 | hp2 | a0001 | c0001 | t0021 | g0104 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01943 | hp1 | a0002 | c0002 | t0082 | g0299 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01943 | hp2 | a0001 | c0001 | t0022 | g0216 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01952 | hp1 | a0002 | c0002 | t0093 | g0088 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01952 | hp2 | a0001 | c0001 | t0070 | g0141 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01975 | hp1 | a0002 | c0003 | t0018 | g0086 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01981 | hp1 | a0002 | c0003 | t0002 | g0265 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01981 | hp2 | a0002 | c0002 | t0091 | g0047 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0267 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02004 | hp1 | a0002 | c0002 | t0015 | g0070 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02004 | hp2 | a0001 | c0001 | t0020 | g0122 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02015 | hp2 | a0002 | c0003 | t0024 | g0269 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0116 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0093 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02055 | hp1 | a0001 | c0001 | t0078 | g0143 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02055 | hp2 | a0001 | c0001 | t0037 | g0285 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02071 | hp1 | a0001 | c0017 | t0001 | g0181 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02071 | hp2 | a0001 | c0001 | t0012 | g0214 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02074 | hp2 | a0001 | c0001 | t0012 | g0119 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02080 | hp1 | a0002 | c0002 | t0096 | g0073 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02080 | hp2 | a0001 | c0001 | t0013 | g0134 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02129 | hp2 | a0002 | c0002 | t0011 | g0048 | EAS | KHV | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02145 | hp1 | a0001 | c0001 | t0031 | g0029 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02145 | hp2 | a0002 | c0003 | t0005 | g0245 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02148 | hp2 | a0002 | c0002 | t0041 | g0071 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02155 | hp1 | a0001 | c0001 | t0013 | g0097 | EAS | CDX | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02258 | hp1 | a0002 | c0003 | t0003 | g0253 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02273 | hp2 | a0001 | c0001 | t0008 | g0053 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02280 | hp1 | a0001 | c0001 | t0068 | g0277 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02451 | hp1 | a0003 | c0004 | t0049 | g0314 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02451 | hp2 | a0002 | c0002 | t0085 | g0136 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02572 | hp2 | a0001 | c0001 | t0036 | g0043 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02602 | hp1 | a0001 | c0001 | t0025 | g0125 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02602 | hp2 | a0002 | c0002 | t0092 | g0087 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02615 | hp1 | a0001 | c0001 | t0060 | g0306 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02615 | hp2 | a0002 | c0002 | t0089 | g0309 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0237 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02630 | hp1 | a0001 | c0001 | t0026 | g0304 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02630 | hp2 | a0003 | c0004 | t0047 | g0287 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0234 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02698 | hp1 | a0002 | c0003 | t0002 | g0228 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02717 | hp1 | a0001 | c0001 | t0026 | g0307 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02717 | hp2 | a0001 | c0001 | t0073 | g0140 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02735 | hp1 | a0002 | c0003 | t0003 | g0024 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0124 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02809 | hp2 | a0002 | c0003 | t0018 | g0085 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02818 | hp2 | a0001 | c0001 | t0026 | g0305 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02886 | hp1 | a0001 | c0001 | t0066 | g0148 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02886 | hp2 | a0002 | c0002 | t0015 | g0290 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02895 | hp1 | a0001 | c0001 | t0072 | g0150 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02922 | hp1 | a0002 | c0003 | t0018 | g0014 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02922 | hp2 | a0002 | c0003 | t0019 | g0028 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02965 | hp2 | a0001 | c0001 | t0037 | g0284 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02976 | hp2 | a0002 | c0002 | t0039 | g0145 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03017 | hp1 | a0001 | c0001 | t0013 | g0120 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03017 | hp2 | a0001 | c0001 | t0064 | g0118 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03041 | hp1 | a0008 | c0015 | t0076 | g0042 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03098 | hp1 | a0001 | c0001 | t0031 | g0029 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0289 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03130 | hp1 | a0001 | c0001 | t0036 | g0041 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03130 | hp2 | a0002 | c0003 | t0032 | g0264 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03139 | hp1 | a0001 | c0001 | t0080 | g0283 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03195 | hp1 | a0001 | c0001 | t0034 | g0279 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03195 | hp2 | a0002 | c0003 | t0018 | g0014 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03209 | hp2 | a0002 | c0002 | t0102 | g0288 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03225 | hp1 | a0002 | c0002 | t0083 | g0121 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0013 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03239 | hp2 | a0002 | c0003 | t0003 | g0274 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03453 | hp1 | a0002 | c0002 | t0043 | g0030 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03453 | hp2 | a0002 | c0003 | t0097 | g0227 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03486 | hp1 | a0002 | c0002 | t0084 | g0310 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03486 | hp2 | a0001 | c0001 | t0071 | g0282 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0011 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03490 | hp2 | a0001 | c0001 | t0023 | g0187 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03491 | hp1 | a0002 | c0002 | t0009 | g0045 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03491 | hp2 | a0009 | c0016 | t0001 | g0193 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03492 | hp1 | a0002 | c0002 | t0009 | g0066 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03492 | hp2 | a0001 | c0001 | t0014 | g0011 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03540 | hp1 | a0002 | c0003 | t0002 | g0255 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03540 | hp2 | a0002 | c0003 | t0018 | g0084 | AFR | GWD | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03579 | hp1 | a0001 | c0001 | t0074 | g0286 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03579 | hp2 | a0003 | c0004 | t0046 | g0315 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0010 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03654 | hp2 | a0002 | c0003 | t0005 | g0275 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03669 | hp1 | a0002 | c0002 | t0009 | g0297 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0132 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03688 | hp1 | a0001 | c0001 | t0081 | g0138 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03688 | hp2 | a0002 | c0002 | t0017 | g0155 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03710 | hp2 | a0002 | c0002 | t0011 | g0302 | SAS | PJL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04115 | hp1 | a0001 | c0001 | t0054 | g0184 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04115 | hp2 | a0002 | c0002 | t0041 | g0062 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04204 | hp1 | a0001 | c0001 | t0103 | g0185 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0218 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04228 | hp1 | a0001 | c0001 | t0023 | g0195 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0024 | SAS | STU | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18522 | hp1 | a0001 | c0001 | t0034 | g0278 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18747 | hp1 | a0002 | c0002 | t0015 | g0198 | EAS | CHB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18906 | hp1 | a0002 | c0002 | t0086 | g0311 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18941 | hp2 | a0001 | c0001 | t0014 | g0215 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18942 | hp1 | a0001 | c0001 | t0099 | g0199 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18945 | hp1 | a0005 | c0005 | t0009 | g0081 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0252 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0063 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18948 | hp1 | a0001 | c0001 | t0062 | g0111 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18948 | hp2 | a0002 | c0002 | t0017 | g0078 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18950 | hp1 | a0001 | c0001 | t0016 | g0204 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18953 | hp2 | a0002 | c0003 | t0003 | g0270 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18954 | hp1 | a0001 | c0001 | t0012 | g0203 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18957 | hp1 | a0010 | c0008 | t0024 | g0031 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18957 | hp2 | a0001 | c0001 | t0020 | g0037 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18959 | hp1 | a0001 | c0001 | t0061 | g0153 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18959 | hp2 | a0001 | c0001 | t0053 | g0208 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18963 | hp1 | a0002 | c0003 | t0002 | g0250 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18965 | hp2 | a0001 | c0001 | t0016 | g0133 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0105 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18966 | hp2 | a0006 | c0006 | t0004 | g0075 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18969 | hp1 | a0002 | c0003 | t0002 | g0259 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18969 | hp2 | a0006 | c0006 | t0009 | g0074 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18970 | hp1 | a0002 | c0013 | t0019 | g0243 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18970 | hp2 | a0001 | c0001 | t0016 | g0183 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18971 | hp2 | a0002 | c0003 | t0005 | g0026 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18973 | hp1 | a0002 | c0003 | t0003 | g0251 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18973 | hp2 | a0001 | c0001 | t0010 | g0038 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18974 | hp1 | a0001 | c0001 | t0035 | g0036 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18975 | hp2 | a0002 | c0002 | t0027 | g0197 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18977 | hp1 | a0002 | c0002 | t0042 | g0091 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18978 | hp2 | a0001 | c0001 | t0038 | g0200 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18979 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18983 | hp1 | a0001 | c0001 | t0016 | g0115 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18983 | hp2 | a0002 | c0003 | t0005 | g0240 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18986 | hp1 | a0002 | c0002 | t0015 | g0050 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18986 | hp2 | a0001 | c0001 | t0014 | g0051 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18990 | hp1 | a0002 | c0003 | t0003 | g0261 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18990 | hp2 | a0011 | c0010 | t0017 | g0083 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18991 | hp2 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18993 | hp2 | a0001 | c0001 | t0021 | g0100 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18994 | hp1 | a0001 | c0001 | t0022 | g0110 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18994 | hp2 | a0002 | c0003 | t0003 | g0242 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18995 | hp2 | a0001 | c0001 | t0079 | g0099 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18997 | hp1 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18997 | hp2 | a0012 | c0018 | t0005 | g0235 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18998 | hp2 | a0013 | c0012 | t0002 | g0248 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18999 | hp1 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19001 | hp1 | a0002 | c0003 | t0003 | g0232 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19001 | hp2 | a0002 | c0002 | t0042 | g0094 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19002 | hp1 | a0002 | c0002 | t0004 | g0013 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19002 | hp2 | a0002 | c0003 | t0002 | g0231 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19003 | hp2 | a0002 | c0003 | t0002 | g0246 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0068 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19010 | hp1 | a0002 | c0003 | t0005 | g0026 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19010 | hp2 | a0001 | c0001 | t0012 | g0126 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19012 | hp1 | a0002 | c0002 | t0028 | g0095 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19030 | hp1 | a0003 | c0014 | t0045 | g0152 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19030 | hp2 | a0002 | c0002 | t0039 | g0312 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19043 | hp2 | a0002 | c0003 | t0019 | g0236 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19056 | hp1 | a0001 | c0001 | t0020 | g0114 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19056 | hp2 | a0005 | c0005 | t0004 | g0080 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19057 | hp1 | a0002 | c0003 | t0003 | g0025 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19057 | hp2 | a0001 | c0001 | t0100 | g0101 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19058 | hp1 | a0002 | c0003 | t0003 | g0244 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19058 | hp2 | a0001 | c0001 | t0025 | g0112 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19060 | hp2 | a0001 | c0001 | t0021 | g0090 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19062 | hp1 | a0001 | c0001 | t0077 | g0061 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19062 | hp2 | a0002 | c0002 | t0015 | g0060 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19063 | hp1 | a0001 | c0001 | t0035 | g0201 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19065 | hp1 | a0001 | c0001 | t0023 | g0180 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0202 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0211 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19068 | hp2 | a0002 | c0002 | t0027 | g0064 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19070 | hp1 | a0014 | c0019 | t0021 | g0117 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19070 | hp2 | a0002 | c0002 | t0028 | g0147 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19074 | hp2 | a0001 | c0001 | t0101 | g0096 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19075 | hp2 | a0001 | c0001 | t0063 | g0219 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19085 | hp2 | a0002 | c0003 | t0002 | g0238 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19086 | hp1 | a0002 | c0002 | t0009 | g0082 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19086 | hp2 | a0001 | c0001 | t0022 | g0137 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19089 | hp1 | a0001 | c0001 | t0098 | g0092 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19089 | hp2 | a0002 | c0003 | t0002 | g0272 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0107 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19090 | hp2 | a0002 | c0003 | t0005 | g0258 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19091 | hp2 | a0002 | c0002 | t0090 | g0069 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19240 | hp1 | a0001 | c0001 | t0065 | g0154 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA19240 | hp2 | a0002 | c0003 | t0058 | g0229 | AFR | YRI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0035 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20805 | hp1 | a0002 | c0003 | t0002 | g0027 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0217 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG01123 | hp2 | a0002 | c0003 | t0003 | g0247 | AMR | CLM | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02109 | hp2 | a0001 | c0001 | t0025 | g0089 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02486 | hp1 | a0001 | c0001 | t0052 | g0225 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02486 | hp2 | a0002 | c0002 | t0009 | g0292 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02559 | hp1 | a0003 | c0004 | t0048 | g0313 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03471 | hp1 | a0002 | c0002 | t0088 | g0308 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG03471 | hp2 | a0002 | c0003 | t0032 | g0263 | AFR | MSL | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18955 | hp1 | a0002 | c0003 | t0059 | g0260 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20300 | hp1 | a0001 | c0001 | t0051 | g0226 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA20300 | hp2 | a0001 | c0001 | t0044 | g0178 | AFR | USA | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| NA21309 | hp2 | a0002 | c0002 | t0087 | g0303 | AFR | LWK | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0057 | g0046 | REF | REF | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0017 | g0298 | REF | REF | IMPG2_chr3_101217546_101325575 | IMPG2 | chr3 | 101217546 | 101325575 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101229574 | G | A | 1 | a0003 | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.3439C>T | p.Pro1147Ser | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/19 | 3642/8352 | 3439/3726 | 1147/1241 | chr3 | 101229574 | |||
| chr3:101231081 | C | T | 1 | a0013 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.3298G>A | p.Val1100Met | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/19 | 3501/8352 | 3298/3726 | 1100/1241 | chr3 | 101231081 | |||
| chr3:101232976 | G | A | 1 | a0009 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.3038C>T | p.Pro1013Leu | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/19 | 3241/8352 | 3038/3726 | 1013/1241 | chr3 | 101232976 | |||
| chr3:101243693 | C | T | 1 | a0007 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.2638G>A | p.Val880Met | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2841/8352 | 2638/3726 | 880/1241 | chr3 | 101243693 | |||
| chr3:101243717 | C | T | 1 | a0008 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2614G>A | p.Val872Ile | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2817/8352 | 2614/3726 | 872/1241 | chr3 | 101243717 | |||
| chr3:101243900 | A | C | 1 | a0005 | 2 | NA18945.hp1 NA19056.hp2 |
missense_variant | MODERATE | c.2431T>G | p.Ser811Ala | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2634/8352 | 2431/3726 | 811/1241 | chr3 | 101243900 | |||
| chr3:101244260 | C | T | 1 | a0011 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.2071G>A | p.Ala691Thr | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2274/8352 | 2071/3726 | 691/1241 | chr3 | 101244260 | |||
| chr3:101244310 | G | A | 5 | a0001 a0004 a0008 others(2): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
missense_variant | MODERATE | c.2021C>T | p.Thr674Ile | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2224/8352 | 2021/3726 | 674/1241 | chr3 | 101244310 | |||
| chr3:101244749 | T | C | 1 | a0012 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1582A>G | p.Ile528Val | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 1785/8352 | 1582/3726 | 528/1241 | chr3 | 101244749 | |||
| chr3:101245963 | G | C | 1 | a0006 | 2 | NA18966.hp2 NA18969.hp2 |
missense_variant | MODERATE | c.1382C>G | p.Thr461Arg | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/19 | 1585/8352 | 1382/3726 | 461/1241 | chr3 | 101245963 | |||
| chr3:101253712 | G | A | 1 | a0004 | 2 | HG01255.hp1 HG01358.hp1 |
missense_variant | MODERATE | c.1223C>T | p.Thr408Met | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/19 | 1426/8352 | 1223/3726 | 408/1241 | chr3 | 101253712 | |||
| chr3:101253716 | C | A | 1 | a0014 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.1219G>T | p.Ala407Ser | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/19 | 1422/8352 | 1219/3726 | 407/1241 | chr3 | 101253716 | |||
| chr3:101320333 | TACCCAGA others(9): Show |
T | 1 | a0010 | 1 | NA18957.hp1 | frameshift_variant | HIGH | c.24_39delGAAGATTTCT others(6): Show |
p.Lys9fs | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/19 | 242/8352 | 24/3726 | 8/1241 | chr3 | 101320333 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101229413 | T | C | 1 | a0003c0009 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.3600A>G | p.Arg1200Arg | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/19 | 3803/8352 | 3600/3726 | 1200/1241 | chr3 | 101229413 | |||
| chr3:101229452 | G | A | 1 | a0002c0013 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.3561C>T | p.Ser1187Ser | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/19 | 3764/8352 | 3561/3726 | 1187/1241 | chr3 | 101229452 | |||
| chr3:101230998 | G | A | 14 | a0001c0001 a0001c0017 a0002c0003 others(11): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
synonymous_variant | LOW | c.3381C>T | p.Leu1127Leu | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/19 | 3584/8352 | 3381/3726 | 1127/1241 | chr3 | 101230998 | |||
| chr3:101244408 | T | C | 1 | a0001c0017 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1923A>G | p.Pro641Pro | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2126/8352 | 1923/3726 | 641/1241 | chr3 | 101244408 | |||
| chr3:101244423 | A | G | 2 | a0003c0004 a0003c0009 |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.1908T>C | p.Asp636Asp | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/19 | 2111/8352 | 1908/3726 | 636/1241 | chr3 | 101244423 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101222643 | T | G | 1 | a0001c0001t0052 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4326A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 4326 | chr3 | 101222643 | ||||||
| chr3:101222848 | A | C | 60 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(57): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*4121T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 4121 | chr3 | 101222848 | ||||||
| chr3:101222995 | T | C | 1 | a0002c0002t0092 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3974A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3974 | chr3 | 101222995 | ||||||
| chr3:101223116 | C | T | 1 | a0001c0001t0079 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3853G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3853 | chr3 | 101223116 | ||||||
| chr3:101223189 | A | T | 82 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(79): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*3780T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3780 | chr3 | 101223189 | ||||||
| chr3:101223455 | G | A | 1 | a0001c0001t0033 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3514C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3514 | chr3 | 101223455 | ||||||
| chr3:101223704 | A | T | 1 | a0001c0001t0055 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3265T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3265 | chr3 | 101223704 | ||||||
| chr3:101223920 | C | T | 3 | a0002c0003t0018 a0002c0003t0058 a0002c0003t0097 |
7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3049G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 3049 | chr3 | 101223920 | ||||||
| chr3:101224006 | A | G | 1 | a0001c0001t0065 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2963T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2963 | chr3 | 101224006 | ||||||
| chr3:101224052 | C | T | 1 | a0001c0001t0062 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2917G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2917 | chr3 | 101224052 | ||||||
| chr3:101224084 | G | T | 2 | a0002c0003t0018 a0002c0003t0097 |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2885C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2885 | chr3 | 101224084 | ||||||
| chr3:101224100 | G | A | 4 | a0001c0001t0037 a0001c0001t0071 a0001c0001t0074 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2869C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2869 | chr3 | 101224100 | ||||||
| chr3:101224316 | A | G | 1 | a0003c0014t0045 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2653T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2653 | chr3 | 101224316 | ||||||
| chr3:101224669 | G | A | 1 | a0001c0001t0055 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2300C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2300 | chr3 | 101224669 | ||||||
| chr3:101224691 | G | C | 6 | a0001c0001t0036 a0001c0001t0065 a0001c0001t0066 others(3): Show |
7 | HG01884.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2278C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2278 | chr3 | 101224691 | ||||||
| chr3:101224727 | C | T | 1 | a0001c0001t0064 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2242G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2242 | chr3 | 101224727 | ||||||
| chr3:101224874 | C | T | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2095G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2095 | chr3 | 101224874 | ||||||
| chr3:101224917 | T | G | 1 | a0002c0003t0059 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 2052 | chr3 | 101224917 | ||||||
| chr3:101225015 | C | T | 7 | a0001c0001t0026 a0001c0001t0031 a0001c0001t0034 others(4): Show |
11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1954 | chr3 | 101225015 | ||||||
| chr3:101225232 | A | G | 14 | a0001c0001t0054 a0002c0003t0002 a0002c0003t0003 others(11): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1737T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1737 | chr3 | 101225232 | ||||||
| chr3:101225369 | G | A | 1 | a0001c0001t0061 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1600C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1600 | chr3 | 101225369 | ||||||
| chr3:101225374 | C | T | 3 | a0002c0003t0018 a0002c0003t0058 a0002c0003t0097 |
7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1595G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1595 | chr3 | 101225374 | ||||||
| chr3:101225380 | T | C | 15 | a0001c0001t0054 a0002c0003t0002 a0002c0003t0003 others(12): Show |
61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1589A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1589 | chr3 | 101225380 | ||||||
| chr3:101225411 | ACACGCAC others(9): Show |
A | 81 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(78): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1542_*1557delAATG others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1542 | chr3 | 101225411 | ||||||
| chr3:101225427 | T | A | 1 | a0001c0001t0056 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1542 | chr3 | 101225427 | ||||||
| chr3:101225687 | G | A | 5 | a0003c0004t0046 a0003c0004t0047 a0003c0004t0048 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1282C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1282 | chr3 | 101225687 | ||||||
| chr3:101225965 | C | T | 2 | a0001c0001t0070 a0001c0001t0078 |
2 | HG01952.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 1004 | chr3 | 101225965 | ||||||
| chr3:101226088 | A | G | 15 | a0001c0001t0054 a0002c0003t0002 a0002c0003t0003 others(12): Show |
61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 881 | chr3 | 101226088 | ||||||
| chr3:101226123 | A | C | 1 | a0001c0001t0053 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*846T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 846 | chr3 | 101226123 | ||||||
| chr3:101226159 | G | A | 2 | a0001c0001t0077 a0002c0003t0097 |
2 | HG03453.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*810C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 810 | chr3 | 101226159 | ||||||
| chr3:101226225 | T | A | 1 | a0002c0002t0094 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 744 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTA | 3 | a0001c0001t0073 a0001c0001t0099 a0002c0002t0093 |
3 | HG01952.hp1 HG02717.hp2 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*742_*743dupTA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATA | 3 | a0001c0001t0007 a0001c0001t0100 a0002c0002t0041 |
12 | HG02148.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*740_*743dupTATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATA | 4 | a0001c0001t0012 a0001c0001t0036 a0001c0001t0074 others(1): Show |
11 | HG02071.hp2 HG02074.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*738_*743dupTATATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(1): Show |
6 | a0001c0001t0010 a0001c0001t0077 a0002c0002t0028 others(3): Show |
14 | HG00639.hp2 HG01070.hp1 HG01169.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*736_*743dupTATATA others(2): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(3): Show |
5 | a0001c0001t0013 a0001c0001t0037 a0001c0001t0078 others(2): Show |
11 | HG00099.hp2 HG00280.hp1 HG02040.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*734_*743dupTATATA others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(5): Show |
4 | a0001c0001t0021 a0001c0001t0079 a0001c0001t0080 others(1): Show |
6 | HG01891.hp2 HG03139.hp1 NA18993.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*732_*743dupTATATA others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(7): Show |
1 | a0001c0001t0016 | 5 | NA18950.hp1 NA18965.hp2 NA18970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*730_*743dupTATATA others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(9): Show |
3 | a0001c0001t0014 a0002c0002t0088 a0002c0002t0096 |
8 | HG01074.hp2 HG02080.hp1 HG03471.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*728_*743dupTATATA others(10): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(11): Show |
2 | a0001c0001t0022 a0002c0002t0089 |
5 | HG00621.hp1 HG01943.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*726_*743dupTATATA others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(13): Show |
1 | a0001c0001t0038 | 2 | HG01261.hp2 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*724_*743dupTATATA others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(25): Show |
1 | a0001c0001t0060 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*743_*744insTATATA others(26): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | T | TTATATAT others(27): Show |
1 | a0001c0001t0031 | 2 | HG02145.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*743_*744insTATATA others(28): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 743 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTA | T | 5 | a0001c0001t0034 a0001c0001t0035 a0002c0002t0015 others(2): Show |
12 | HG00140.hp2 HG02004.hp1 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*743delTA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 742 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATA | T | 9 | a0001c0001t0025 a0001c0001t0068 a0001c0001t0069 others(6): Show |
17 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*740_*743delTATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 740 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATA | T | 4 | a0001c0001t0006 a0001c0001t0066 a0002c0002t0027 others(1): Show |
14 | HG01099.hp1 HG01978.hp1 HG02148.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*738_*743delTATATA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 738 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(1): Show |
T | 8 | a0001c0001t0033 a0001c0001t0064 a0001c0001t0065 others(5): Show |
14 | HG00621.hp2 HG01256.hp2 HG01258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*736_*743delTATATA others(2): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 736 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(3): Show |
T | 5 | a0001c0001t0062 a0001c0001t0063 a0002c0002t0011 others(2): Show |
13 | HG00280.hp2 HG00642.hp2 HG01071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*734_*743delTATATA others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 734 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(5): Show |
T | 3 | a0002c0002t0040 a0002c0003t0024 a0010c0008t0024 |
5 | HG00423.hp1 HG01106.hp2 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*732_*743delTATATA others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 732 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(7): Show |
T | 3 | a0002c0002t0085 a0002c0003t0005 a0012c0018t0005 |
10 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*730_*743delTATATA others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 730 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(9): Show |
T | 3 | a0001c0001t0061 a0002c0002t0084 a0002c0003t0003 |
18 | HG00140.hp1 HG00408.hp2 HG00733.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*728_*743delTATATA others(10): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 728 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(11): Show |
T | 3 | a0002c0003t0002 a0002c0003t0059 a0013c0012t0002 |
23 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*726_*743delTATATA others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 726 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(13): Show |
T | 3 | a0002c0003t0019 a0002c0003t0058 a0002c0013t0019 |
5 | HG01106.hp1 HG02922.hp2 NA18970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*724_*743delTATATA others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 724 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(15): Show |
T | 2 | a0003c0004t0048 a0003c0014t0045 |
2 | HG02559.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*722_*743delTATATA others(16): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 722 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0081 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718_*743delTATATA others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 718 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(21): Show |
T | 2 | a0001c0001t0008 a0001c0001t0029 |
10 | HG00642.hp1 HG01123.hp1 HG01167.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*743delTATATA others(22): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 716 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(23): Show |
T | 2 | a0002c0003t0097 a0003c0009t0050 |
2 | HG01891.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*714_*743delTATATA others(24): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 714 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(25): Show |
T | 2 | a0002c0002t0083 a0002c0003t0018 |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*712_*743delTATATA others(26): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 712 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(27): Show |
T | 1 | a0003c0004t0047 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710_*743delTATATA others(28): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 710 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(29): Show |
T | 2 | a0001c0001t0023 a0003c0004t0046 |
4 | HG03490.hp2 HG03579.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*708_*743delTATATA others(30): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 708 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(31): Show |
T | 11 | a0001c0001t0001 a0001c0001t0030 a0001c0001t0044 others(8): Show |
101 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*706_*743delTATATA others(32): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 706 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(33): Show |
T | 2 | a0001c0001t0051 a0001c0001t0052 |
2 | HG02486.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*704_*743delTATATA others(34): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 704 | chr3 | 101226225 | ||||||
| chr3:101226225 | TTATATAT others(35): Show |
T | 1 | a0002c0002t0091 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702_*743delTATATA others(36): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 702 | chr3 | 101226225 | ||||||
| chr3:101226241 | A | ATTTATAT others(65): Show |
1 | a0001c0001t0026 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727_*728insAATATA others(66): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 727 | chr3 | 101226241 | ||||||
| chr3:101226241 | A | ATTTATAT others(29): Show |
1 | a0001c0001t0026 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*727_*728insAATATA others(30): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 727 | chr3 | 101226241 | ||||||
| chr3:101226243 | A | T | 3 | a0001c0001t0026 a0001c0001t0031 a0001c0001t0060 |
4 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 726 | chr3 | 101226243 | ||||||
| chr3:101226260 | T | TATATATA others(27): Show |
1 | a0001c0001t0026 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*708_*709insTTATAT others(28): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 708 | chr3 | 101226260 | ||||||
| chr3:101226265 | A | G | 1 | a0001c0001t0081 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 704 | chr3 | 101226265 | ||||||
| chr3:101226266 | T | C | 1 | a0001c0001t0081 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 703 | chr3 | 101226266 | ||||||
| chr3:101226305 | A | G | 1 | a0002c0002t0082 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*664T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 664 | chr3 | 101226305 | ||||||
| chr3:101226334 | A | T | 1 | a0002c0002t0090 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 635 | chr3 | 101226334 | ||||||
| chr3:101226401 | G | T | 82 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(79): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*568C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 568 | chr3 | 101226401 | ||||||
| chr3:101226523 | C | T | 5 | a0003c0004t0046 a0003c0004t0047 a0003c0004t0048 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*446G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 446 | chr3 | 101226523 | ||||||
| chr3:101226525 | C | T | 4 | a0003c0004t0046 a0003c0004t0047 a0003c0004t0048 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*444G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 444 | chr3 | 101226525 | ||||||
| chr3:101226543 | C | T | 1 | a0001c0001t0029 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*426G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 426 | chr3 | 101226543 | ||||||
| chr3:101226589 | G | T | 92 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(89): Show |
303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*380C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 380 | chr3 | 101226589 | ||||||
| chr3:101226669 | A | C | 1 | a0003c0014t0045 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 300 | chr3 | 101226669 | ||||||
| chr3:101226709 | T | C | 2 | a0002c0003t0018 a0002c0003t0097 |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*260A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 260 | chr3 | 101226709 | ||||||
| chr3:101226741 | A | G | 1 | a0001c0001t0044 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 228 | chr3 | 101226741 | ||||||
| chr3:101226819 | G | GA | 5 | a0001c0001t0098 a0001c0001t0099 a0001c0001t0100 others(2): Show |
5 | HG03209.hp2 NA18942.hp1 NA19057.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*149dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 149 | chr3 | 101226819 | ||||||
| chr3:101226882 | T | G | 1 | a0001c0001t0103 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 19/19 | 87 | chr3 | 101226882 | ||||||
| chr3:101320485 | A | G | 1 | a0002c0002t0043 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/19 | 113 | chr3 | 101320485 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:101227139 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3714-158T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227139 | |||||||
| chr3:101227140 | T | A | 5 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3714-159A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227140 | |||||||
| chr3:101227326 | G | A | 1 | a0002c0003t0003g0251 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3714-345C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227326 | |||||||
| chr3:101227391 | C | G | 1 | a0002c0003t0005g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3714-410G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227391 | |||||||
| chr3:101227569 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3714-588A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227569 | |||||||
| chr3:101227570 | G | A | 1 | a0012c0018t0005g0235 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3714-589C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227570 | |||||||
| chr3:101227898 | T | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3713+899A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227898 | |||||||
| chr3:101227936 | A | G | 1 | a0001c0001t0013g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3713+861T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227936 | |||||||
| chr3:101227964 | T | C | 1 | a0001c0001t0077g0061 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3713+833A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101227964 | |||||||
| chr3:101228014 | C | T | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3713+783G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228014 | |||||||
| chr3:101228021 | C | T | 5 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3713+776G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228021 | |||||||
| chr3:101228189 | T | C | 1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3713+608A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228189 | |||||||
| chr3:101228367 | A | C | 1 | a0002c0003t0003g0232 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3713+430T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228367 | |||||||
| chr3:101228412 | G | T | 1 | a0002c0003t0002g0266 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3713+385C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228412 | |||||||
| chr3:101228419 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3713+378T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228419 | |||||||
| chr3:101228475 | G | A | 1 | a0002c0003t0018g0086 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3713+322C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228475 | |||||||
| chr3:101228621 | G | A | 5 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3713+176C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228621 | |||||||
| chr3:101228730 | G | T | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3713+67C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 18/18 | chr3 | 101228730 | |||||||
| chr3:101228970 | C | T | 1 | a0002c0003t0058g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3634-94G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101228970 | |||||||
| chr3:101229138 | C | CA | 7 | a0002c0002t0009g0066 a0002c0002t0102g0288 a0002c0003t0002g0271 others(4): Show |
8 | HG00673.hp1 HG01106.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3633+241dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229138 | |||||||
| chr3:101229138 | CA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
112 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.3633+241delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229138 | |||||||
| chr3:101229138 | CAA | C | 106 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 others(103): Show |
114 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.3633+240_3633+241d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229138 | |||||||
| chr3:101229156 | G | A | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+224C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229156 | |||||||
| chr3:101229167 | G | A | 5 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(2): Show |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+213C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 17/18 | chr3 | 101229167 | |||||||
| chr3:101229763 | TATC | T | 5 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(2): Show |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3423-176_3423-174d others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101229763 | |||||||
| chr3:101230076 | G | A | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3423-486C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230076 | |||||||
| chr3:101230156 | A | G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3423-566T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230156 | |||||||
| chr3:101230163 | C | T | 1 | a0002c0003t0067g0249 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3423-573G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230163 | |||||||
| chr3:101230369 | A | G | 1 | a0002c0002t0085g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3422+588T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230369 | |||||||
| chr3:101230487 | T | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3422+470A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230487 | |||||||
| chr3:101230491 | T | C | 1 | a0001c0001t0020g0213 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3422+466A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230491 | |||||||
| chr3:101230582 | T | C | 2 | a0002c0003t0002g0246 a0002c0003t0003g0252 |
2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.3422+375A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230582 | |||||||
| chr3:101230824 | C | A | 85 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 others(82): Show |
92 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.3422+133G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230824 | |||||||
| chr3:101230907 | T | C | 1 | a0002c0003t0003g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3422+50A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 16/18 | chr3 | 101230907 | |||||||
| chr3:101231190 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3234-45G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231190 | |||||||
| chr3:101231317 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3234-172T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231317 | |||||||
| chr3:101231335 | C | T | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3234-190G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231335 | |||||||
| chr3:101231626 | A | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
75 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.3234-481T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231626 | |||||||
| chr3:101231628 | G | A | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3234-483C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231628 | |||||||
| chr3:101231831 | T | C | 1 | a0002c0002t0015g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3234-686A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101231831 | |||||||
| chr3:101232223 | A | AT | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
221 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.3233+557dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232223 | |||||||
| chr3:101232223 | A | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3233+558T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232223 | |||||||
| chr3:101232234 | A | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3233+547T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232234 | |||||||
| chr3:101232238 | A | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3233+543T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232238 | |||||||
| chr3:101232284 | C | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
204 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3233+497G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232284 | |||||||
| chr3:101232330 | C | T | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3233+451G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232330 | |||||||
| chr3:101232382 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3233+399A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232382 | |||||||
| chr3:101232461 | C | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3233+320G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232461 | |||||||
| chr3:101232611 | T | C | 5 | a0001c0001t0012g0126 a0001c0001t0012g0203 a0001c0001t0013g0134 others(2): Show |
5 | HG02080.hp2 NA18954.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3233+170A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232611 | |||||||
| chr3:101232726 | T | C | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3233+55A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232726 | |||||||
| chr3:101232735 | GAAATATC others(31): Show |
G | 1 | a0001c0001t0001g0169 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.3233+8_3233+45delG others(37): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 15/18 | chr3 | 101232735 | |||||||
| chr3:101233231 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3023-240C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233231 | |||||||
| chr3:101233292 | C | G | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3023-301G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233292 | |||||||
| chr3:101233336 | T | C | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-345A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233336 | |||||||
| chr3:101233385 | T | C | 2 | a0001c0001t0010g0035 a0001c0001t0014g0011 |
3 | HG03490.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3023-394A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233385 | |||||||
| chr3:101233423 | A | G | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-432T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233423 | |||||||
| chr3:101233446 | G | C | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-455C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233446 | |||||||
| chr3:101233465 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3023-474G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233465 | |||||||
| chr3:101233597 | C | G | 2 | a0002c0003t0005g0254 a0002c0003t0005g0256 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3023-606G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233597 | |||||||
| chr3:101233848 | T | C | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-857A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233848 | |||||||
| chr3:101233934 | A | G | 1 | a0002c0003t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3023-943T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233934 | |||||||
| chr3:101233981 | A | G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-990T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101233981 | |||||||
| chr3:101234273 | G | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-1282C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234273 | |||||||
| chr3:101234368 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
204 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3023-1377A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234368 | |||||||
| chr3:101234473 | C | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0034 others(3): Show |
9 | HG02559.hp2 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3023-1482G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234473 | |||||||
| chr3:101234582 | T | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-1591A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234582 | |||||||
| chr3:101234598 | G | T | 1 | a0002c0003t0002g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3023-1607C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234598 | |||||||
| chr3:101234681 | A | G | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-1690T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234681 | |||||||
| chr3:101234707 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0162 |
2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3023-1716C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234707 | |||||||
| chr3:101234710 | A | G | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-1719T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234710 | |||||||
| chr3:101234712 | G | C | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-1721C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234712 | |||||||
| chr3:101234941 | T | G | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-1950A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234941 | |||||||
| chr3:101234998 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0165 |
4 | HG02738.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3023-2007G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101234998 | |||||||
| chr3:101235005 | A | G | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-2014T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235005 | |||||||
| chr3:101235034 | T | C | 5 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-2043A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235034 | |||||||
| chr3:101235090 | C | T | 1 | a0002c0003t0058g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3023-2099G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235090 | |||||||
| chr3:101235104 | T | A | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-2113A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235104 | |||||||
| chr3:101235210 | T | C | 1 | a0001c0001t0022g0110 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3023-2219A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235210 | |||||||
| chr3:101235338 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3023-2347A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235338 | |||||||
| chr3:101235558 | C | T | 3 | a0001c0001t0051g0226 a0001c0001t0052g0225 a0002c0003t0003g0253 |
3 | HG02258.hp1 HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3023-2567G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235558 | |||||||
| chr3:101235695 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3023-2704C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235695 | |||||||
| chr3:101235776 | G | A | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3023-2785C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235776 | |||||||
| chr3:101235828 | T | C | 1 | a0001c0001t0025g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3023-2837A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101235828 | |||||||
| chr3:101236084 | T | C | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-3093A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236084 | |||||||
| chr3:101236161 | G | A | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-3170C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236161 | |||||||
| chr3:101236251 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3023-3260C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236251 | |||||||
| chr3:101236302 | C | T | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-3311G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236302 | |||||||
| chr3:101236415 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3023-3424C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236415 | |||||||
| chr3:101236451 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3023-3460G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236451 | |||||||
| chr3:101236460 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
204 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3023-3469A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236460 | |||||||
| chr3:101236485 | T | C | 3 | a0001c0001t0036g0041 a0001c0001t0036g0043 a0008c0015t0076g0042 |
3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3023-3494A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236485 | |||||||
| chr3:101236517 | G | T | 1 | a0014c0019t0021g0117 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3023-3526C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236517 | |||||||
| chr3:101236530 | G | A | 1 | a0002c0002t0017g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3023-3539C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236530 | |||||||
| chr3:101236572 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3023-3581C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236572 | |||||||
| chr3:101236674 | T | C | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-3683A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236674 | |||||||
| chr3:101236696 | G | A | 1 | a0001c0001t0051g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3023-3705C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236696 | |||||||
| chr3:101236747 | C | T | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3023-3756G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236747 | |||||||
| chr3:101236748 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3023-3757T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236748 | |||||||
| chr3:101236808 | G | GTTTGTT | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3023-3823_3023-381 others(10): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236808 | |||||||
| chr3:101236916 | T | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-3925A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236916 | |||||||
| chr3:101236925 | G | A | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3023-3934C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101236925 | |||||||
| chr3:101237013 | C | T | 1 | a0001c0001t0013g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3023-4022G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237013 | |||||||
| chr3:101237096 | G | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-4105C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237096 | |||||||
| chr3:101237227 | A | G | 1 | a0002c0003t0003g0247 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3023-4236T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237227 | |||||||
| chr3:101237286 | G | A | 10 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(7): Show |
11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3023-4295C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237286 | |||||||
| chr3:101237331 | G | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3023-4340C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237331 | |||||||
| chr3:101237356 | C | G | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3023-4365G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101237356 | |||||||
| chr3:101238179 | T | C | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+4509A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238179 | |||||||
| chr3:101238206 | A | G | 2 | a0006c0006t0004g0075 a0006c0006t0009g0074 |
2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.3022+4482T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238206 | |||||||
| chr3:101238476 | C | T | 3 | a0002c0002t0004g0144 a0002c0002t0028g0095 a0002c0002t0042g0094 |
3 | HG00438.hp2 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3022+4212G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238476 | |||||||
| chr3:101238483 | C | T | 2 | a0001c0001t0012g0119 a0001c0001t0014g0215 |
2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4205G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238483 | |||||||
| chr3:101238496 | A | G | 2 | a0001c0001t0012g0119 a0001c0001t0014g0215 |
2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4192T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238496 | |||||||
| chr3:101238498 | C | T | 2 | a0001c0001t0012g0119 a0001c0001t0014g0215 |
2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4190G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238498 | |||||||
| chr3:101238514 | G | A | 2 | a0001c0001t0012g0119 a0001c0001t0014g0215 |
2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3022+4174C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238514 | |||||||
| chr3:101238610 | A | T | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+4078T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238610 | |||||||
| chr3:101238816 | G | A | 5 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(2): Show |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3872C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238816 | |||||||
| chr3:101238837 | T | C | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3851A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238837 | |||||||
| chr3:101238911 | A | T | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3022+3777T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238911 | |||||||
| chr3:101238954 | T | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3022+3734A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238954 | |||||||
| chr3:101238973 | C | T | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3715G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101238973 | |||||||
| chr3:101239174 | GCAATCTA others(39): Show |
G | 4 | a0001c0001t0007g0005 a0001c0001t0007g0106 a0001c0001t0007g0107 others(1): Show |
6 | NA18946.hp2 NA18947.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.3022+3468_3022+351 others(50): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239174 | |||||||
| chr3:101239175 | C | T | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3513G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239175 | |||||||
| chr3:101239280 | T | C | 1 | a0001c0001t0052g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3022+3408A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239280 | |||||||
| chr3:101239311 | T | C | 1 | a0002c0003t0005g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3022+3377A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239311 | |||||||
| chr3:101239410 | C | T | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+3278G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239410 | |||||||
| chr3:101239451 | T | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3022+3237A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239451 | |||||||
| chr3:101239563 | T | C | 1 | a0002c0002t0004g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3022+3125A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239563 | |||||||
| chr3:101239588 | A | G | 1 | a0002c0003t0058g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3022+3100T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239588 | |||||||
| chr3:101239633 | C | T | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3022+3055G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239633 | |||||||
| chr3:101239766 | G | A | 2 | a0002c0002t0009g0292 a0002c0002t0027g0293 |
2 | HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3022+2922C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239766 | |||||||
| chr3:101239805 | G | T | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3022+2883C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239805 | |||||||
| chr3:101239868 | A | G | 1 | a0002c0003t0058g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3022+2820T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239868 | |||||||
| chr3:101239915 | G | A | 1 | a0002c0003t0003g0244 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3022+2773C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239915 | |||||||
| chr3:101239930 | C | T | 1 | a0002c0002t0039g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3022+2758G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101239930 | |||||||
| chr3:101240016 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3022+2672C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240016 | |||||||
| chr3:101240067 | TA | T | 7 | a0001c0001t0001g0163 a0001c0001t0065g0154 a0003c0004t0046g0315 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3022+2620delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240067 | |||||||
| chr3:101240125 | A | T | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3022+2563T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240125 | |||||||
| chr3:101240126 | T | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3022+2562A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240126 | |||||||
| chr3:101240176 | C | T | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3022+2512G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240176 | |||||||
| chr3:101240190 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3022+2498C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240190 | |||||||
| chr3:101240227 | C | T | 6 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(3): Show |
7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3022+2461G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240227 | |||||||
| chr3:101240230 | ACCTCAGC | A | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3022+2451_3022+245 others(11): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240230 | |||||||
| chr3:101240325 | C | T | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3022+2363G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240325 | |||||||
| chr3:101240496 | A | G | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3022+2192T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240496 | |||||||
| chr3:101240518 | A | T | 1 | a0001c0001t0073g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3022+2170T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240518 | |||||||
| chr3:101240536 | T | C | 1 | a0001c0001t0073g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3022+2152A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240536 | |||||||
| chr3:101240975 | T | C | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3022+1713A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101240975 | |||||||
| chr3:101241452 | T | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3022+1236A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241452 | |||||||
| chr3:101241633 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3022+1055A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241633 | |||||||
| chr3:101241798 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0057 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.3022+890A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241798 | |||||||
| chr3:101241833 | G | A | 1 | a0002c0002t0091g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3022+855C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101241833 | |||||||
| chr3:101242035 | GA | G | 12 | a0001c0001t0012g0203 a0001c0001t0013g0134 a0001c0001t0052g0225 others(9): Show |
12 | HG01891.hp1 HG02080.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.3022+652delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242035 | |||||||
| chr3:101242051 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3022+637T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242051 | |||||||
| chr3:101242315 | A | T | 6 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(3): Show |
7 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3022+373T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242315 | |||||||
| chr3:101242640 | T | C | 1 | a0002c0002t0083g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3022+48A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 14/18 | chr3 | 101242640 | |||||||
| chr3:101242964 | A | G | 1 | a0002c0003t0002g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2803-57T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101242964 | |||||||
| chr3:101243061 | C | T | 2 | a0001c0001t0037g0284 a0001c0001t0080g0283 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2803-154G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243061 | |||||||
| chr3:101243239 | G | A | 6 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2802+290C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243239 | |||||||
| chr3:101243310 | T | G | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2802+219A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243310 | |||||||
| chr3:101243394 | A | G | 1 | a0001c0001t0044g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2802+135T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 13/18 | chr3 | 101243394 | |||||||
| chr3:101244807 | T | G | 1 | a0001c0001t0007g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1544-20A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101244807 | |||||||
| chr3:101244917 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
105 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1544-130A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101244917 | |||||||
| chr3:101244995 | C | T | 2 | a0002c0003t0032g0263 a0002c0003t0032g0264 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1544-208G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101244995 | |||||||
| chr3:101245013 | G | C | 1 | a0001c0001t0055g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1544-226C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245013 | |||||||
| chr3:101245040 | G | GT | 56 | a0001c0001t0001g0016 a0001c0001t0012g0203 a0001c0001t0013g0134 others(53): Show |
64 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1544-254dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245040 | |||||||
| chr3:101245040 | GT | G | 8 | a0001c0001t0014g0139 a0002c0003t0058g0229 a0003c0004t0046g0315 others(5): Show |
8 | HG01074.hp2 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544-254delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245040 | |||||||
| chr3:101245127 | A | C | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1544-340T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245127 | |||||||
| chr3:101245168 | C | T | 2 | a0002c0002t0088g0308 a0002c0002t0089g0309 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1544-381G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245168 | |||||||
| chr3:101245226 | T | C | 5 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(2): Show |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544-439A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245226 | |||||||
| chr3:101245421 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1543+381G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245421 | |||||||
| chr3:101245549 | A | G | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543+253T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245549 | |||||||
| chr3:101245557 | T | C | 1 | a0002c0002t0004g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1543+245A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245557 | |||||||
| chr3:101245755 | G | A | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543+47C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 12/18 | chr3 | 101245755 | |||||||
| chr3:101246388 | A | AT | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-284dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246388 | |||||||
| chr3:101246664 | A | G | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0222 others(2): Show |
5 | HG01978.hp2 HG02109.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-559T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246664 | |||||||
| chr3:101246702 | T | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1240-597A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246702 | |||||||
| chr3:101246707 | C | T | 1 | a0001c0001t0010g0035 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1240-602G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246707 | |||||||
| chr3:101246810 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1240-705A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101246810 | |||||||
| chr3:101247092 | T | C | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-987A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247092 | |||||||
| chr3:101247097 | T | TA | 89 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 others(86): Show |
96 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1240-993dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247097 | |||||||
| chr3:101247097 | TA | T | 14 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(11): Show |
15 | HG01106.hp1 HG02055.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1240-993delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247097 | |||||||
| chr3:101247234 | G | A | 8 | a0002c0003t0058g0229 a0002c0003t0097g0227 a0003c0004t0046g0315 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240-1129C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247234 | |||||||
| chr3:101247366 | T | C | 8 | a0002c0003t0058g0229 a0002c0003t0097g0227 a0003c0004t0046g0315 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240-1261A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247366 | |||||||
| chr3:101247416 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0222 others(1): Show |
4 | HG01978.hp2 HG02293.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-1311C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247416 | |||||||
| chr3:101247419 | G | A | 3 | a0001c0001t0036g0041 a0001c0001t0036g0043 a0008c0015t0076g0042 |
3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1240-1314C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247419 | |||||||
| chr3:101247468 | A | T | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1240-1363T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247468 | |||||||
| chr3:101247525 | C | T | 1 | a0001c0001t0020g0114 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1240-1420G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247525 | |||||||
| chr3:101247537 | T | C | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-1432A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247537 | |||||||
| chr3:101247602 | TA | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1240-1498delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247602 | |||||||
| chr3:101247602 | TAA | T | 5 | a0002c0003t0002g0246 a0002c0003t0018g0014 a0002c0003t0018g0084 others(2): Show |
6 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-1499_1240-149 others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247602 | |||||||
| chr3:101247722 | T | C | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1240-1617A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247722 | |||||||
| chr3:101247788 | T | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1240-1683A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247788 | |||||||
| chr3:101247952 | C | G | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1240-1847G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101247952 | |||||||
| chr3:101248090 | A | G | 5 | a0002c0003t0002g0271 a0002c0003t0002g0272 a0002c0003t0003g0270 others(2): Show |
5 | HG00673.hp1 HG02015.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240-1985T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248090 | |||||||
| chr3:101248098 | A | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1240-1993T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248098 | |||||||
| chr3:101248165 | A | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0175 others(1): Show |
9 | NA18747.hp2 NA18942.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-2060T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248165 | |||||||
| chr3:101248806 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1240-2701G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248806 | |||||||
| chr3:101248856 | C | T | 1 | a0003c0004t0048g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1240-2751G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101248856 | |||||||
| chr3:101249022 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1240-2917G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249022 | |||||||
| chr3:101249076 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
216 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1240-2971T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249076 | |||||||
| chr3:101249204 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(49): Show |
73 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1240-3099G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249204 | |||||||
| chr3:101249262 | G | A | 12 | a0001c0001t0036g0041 a0001c0001t0036g0043 a0001c0001t0065g0154 others(9): Show |
13 | HG01884.hp1 HG01975.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-3157C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249262 | |||||||
| chr3:101249333 | A | C | 2 | a0001c0001t0007g0129 a0002c0002t0083g0121 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1240-3228T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249333 | |||||||
| chr3:101249794 | C | CA | 63 | a0001c0001t0006g0124 a0001c0001t0037g0284 a0001c0001t0037g0285 others(60): Show |
70 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1240-3690dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249794 | |||||||
| chr3:101249794 | CA | C | 12 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(9): Show |
14 | HG01975.hp1 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240-3690delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249794 | |||||||
| chr3:101249937 | G | A | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1239+3759C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249937 | |||||||
| chr3:101249976 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1239+3720G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101249976 | |||||||
| chr3:101250176 | T | C | 1 | a0001c0001t0008g0217 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1239+3520A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250176 | |||||||
| chr3:101250363 | G | T | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1239+3333C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250363 | |||||||
| chr3:101250508 | C | T | 6 | a0002c0002t0039g0312 a0002c0002t0043g0030 a0002c0002t0084g0310 others(3): Show |
6 | HG02615.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1239+3188G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250508 | |||||||
| chr3:101250952 | A | G | 3 | a0002c0003t0002g0255 a0002c0003t0005g0254 a0002c0003t0005g0256 |
3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1239+2744T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250952 | |||||||
| chr3:101250983 | A | G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239+2713T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101250983 | |||||||
| chr3:101251066 | A | G | 1 | a0001c0001t0007g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1239+2630T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251066 | |||||||
| chr3:101251073 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1239+2623T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251073 | |||||||
| chr3:101251218 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1239+2478T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251218 | |||||||
| chr3:101251396 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
74 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1239+2300A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251396 | |||||||
| chr3:101251401 | T | TA | 4 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0052g0225 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+2294dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251401 | |||||||
| chr3:101251435 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1239+2261T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251435 | |||||||
| chr3:101251568 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0057 others(3): Show |
7 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+2128A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251568 | |||||||
| chr3:101251657 | G | T | 10 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(7): Show |
11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239+2039C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251657 | |||||||
| chr3:101251925 | G | A | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+1771C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101251925 | |||||||
| chr3:101252011 | T | A | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+1685A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252011 | |||||||
| chr3:101252033 | C | A | 2 | a0002c0002t0009g0045 a0002c0002t0009g0066 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1239+1663G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252033 | |||||||
| chr3:101252076 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
230 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1239+1620T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252076 | |||||||
| chr3:101252078 | C | T | 2 | a0001c0001t0012g0119 a0001c0001t0014g0215 |
2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1239+1618G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252078 | |||||||
| chr3:101252122 | C | T | 1 | a0001c0001t0044g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1239+1574G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252122 | |||||||
| chr3:101252130 | A | ACAGC | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+1565_1239+156 others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252130 | |||||||
| chr3:101252194 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1239+1502A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252194 | |||||||
| chr3:101252210 | A | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239+1486T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252210 | |||||||
| chr3:101252296 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1239+1400C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252296 | |||||||
| chr3:101252337 | C | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1239+1359G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252337 | |||||||
| chr3:101252474 | A | G | 3 | a0002c0002t0004g0063 a0002c0002t0015g0050 a0002c0002t0027g0064 |
3 | NA18947.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1239+1222T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252474 | |||||||
| chr3:101252656 | C | T | 1 | a0001c0001t0056g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1239+1040G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252656 | |||||||
| chr3:101252834 | C | T | 1 | a0003c0004t0049g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1239+862G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252834 | |||||||
| chr3:101252945 | A | G | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+751T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101252945 | |||||||
| chr3:101253085 | G | A | 1 | a0002c0002t0040g0300 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1239+611C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253085 | |||||||
| chr3:101253106 | A | T | 2 | a0001c0001t0034g0278 a0001c0001t0034g0279 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1239+590T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253106 | |||||||
| chr3:101253234 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1239+462C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253234 | |||||||
| chr3:101253235 | A | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1239+461T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253235 | |||||||
| chr3:101253237 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1239+459T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253237 | |||||||
| chr3:101253327 | G | C | 1 | a0001c0001t0006g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1239+369C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253327 | |||||||
| chr3:101253335 | C | T | 3 | a0001c0001t0033g0052 a0001c0001t0033g0158 a0001c0001t0064g0118 |
3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1239+361G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253335 | |||||||
| chr3:101253402 | T | C | 5 | a0002c0002t0009g0082 a0002c0002t0015g0198 a0005c0005t0004g0080 others(2): Show |
5 | NA18747.hp1 NA18945.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+294A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253402 | |||||||
| chr3:101253460 | C | A | 2 | a0001c0001t0012g0203 a0001c0001t0013g0134 |
2 | HG02080.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1239+236G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253460 | |||||||
| chr3:101253583 | G | A | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+113C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253583 | |||||||
| chr3:101253662 | G | C | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+34C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 11/18 | chr3 | 101253662 | |||||||
| chr3:101254014 | A | G | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1154-233T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254014 | |||||||
| chr3:101254301 | A | T | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-520T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254301 | |||||||
| chr3:101254396 | T | C | 3 | a0001c0001t0013g0120 a0001c0001t0013g0123 a0001c0001t0020g0122 |
3 | HG00280.hp1 HG02004.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1154-615A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254396 | |||||||
| chr3:101254457 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1154-676A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254457 | |||||||
| chr3:101254613 | A | G | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-832T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254613 | |||||||
| chr3:101254703 | A | C | 1 | a0002c0002t0017g0078 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1154-922T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254703 | |||||||
| chr3:101254838 | C | T | 1 | a0002c0002t0091g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1154-1057G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254838 | |||||||
| chr3:101254874 | G | A | 1 | a0001c0001t0035g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1154-1093C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101254874 | |||||||
| chr3:101255130 | G | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1154-1349C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255130 | |||||||
| chr3:101255174 | A | C | 1 | a0001c0001t0014g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1154-1393T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255174 | |||||||
| chr3:101255280 | T | G | 1 | a0001c0001t0012g0119 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1154-1499A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255280 | |||||||
| chr3:101255515 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1154-1734C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255515 | |||||||
| chr3:101255547 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0165 |
4 | HG02738.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1766C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255547 | |||||||
| chr3:101255612 | C | T | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-1831G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255612 | |||||||
| chr3:101255779 | C | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1153+1750G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255779 | |||||||
| chr3:101255886 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1153+1643A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255886 | |||||||
| chr3:101255895 | T | C | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+1634A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255895 | |||||||
| chr3:101255918 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0044 others(8): Show |
19 | HG00597.hp1 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1153+1611A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255918 | |||||||
| chr3:101255988 | T | TA | 6 | a0002c0002t0039g0312 a0002c0002t0043g0030 a0002c0002t0084g0310 others(3): Show |
6 | HG02615.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1540dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255988 | |||||||
| chr3:101255988 | TA | T | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+1540delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255988 | |||||||
| chr3:101255998 | G | A | 1 | a0001c0001t0052g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+1531C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101255998 | |||||||
| chr3:101256002 | G | A | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1153+1527C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256002 | |||||||
| chr3:101256064 | AAAAAG | A | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1153+1460_1153+146 others(9): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256064 | |||||||
| chr3:101256075 | AAAAGAAA others(28): Show |
A | 1 | a0001c0001t0100g0101 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1153+1419_1153+145 others(39): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256075 | |||||||
| chr3:101256080 | AAAAGAAA others(11): Show |
A | 1 | a0001c0001t0001g0207 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1153+1431_1153+144 others(22): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256080 | |||||||
| chr3:101256114 | G | A | 2 | a0001c0001t0001g0191 a0009c0016t0001g0193 |
2 | HG01175.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1153+1415C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256114 | |||||||
| chr3:101256114 | GA | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0173 |
3 | NA18965.hp1 NA19066.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1153+1414delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256114 | |||||||
| chr3:101256116 | A | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0009c0016t0001g0193 |
3 | HG01175.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1153+1413T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256116 | |||||||
| chr3:101256122 | A | G | 2 | a0001c0001t0001g0191 a0009c0016t0001g0193 |
2 | HG01175.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1153+1407T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256122 | |||||||
| chr3:101256126 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0009c0016t0001g0193 |
3 | HG01175.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1153+1403C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256126 | |||||||
| chr3:101256132 | GAAAGAAA others(6): Show |
G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1384_1153+139 others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256132 | |||||||
| chr3:101256144 | G | A | 3 | a0002c0002t0083g0121 a0003c0004t0046g0315 a0009c0016t0001g0193 |
3 | HG03225.hp1 HG03491.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1153+1385C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256144 | |||||||
| chr3:101256144 | G | GA | 2 | a0001c0001t0001g0006 a0003c0004t0048g0313 |
3 | HG02559.hp1 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1153+1384dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256144 | |||||||
| chr3:101256145 | A | AAAAG | 68 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0018 others(65): Show |
68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1153+1380_1153+138 others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAAGAAA others(1): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0020 others(33): Show |
36 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1153+1376_1153+138 others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAAGAAA others(5): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0192 others(15): Show |
19 | HG00642.hp1 HG01167.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1153+1372_1153+138 others(16): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAAGAAA others(9): Show |
1 | a0001c0001t0012g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1153+1368_1153+138 others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAG | 3 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0038g0200 |
3 | HG01175.hp1 NA18978.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1153+1383_1153+138 others(7): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAGAAAG others(4): Show |
1 | a0002c0003t0002g0246 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAGAAAG others(8): Show |
1 | a0002c0002t0027g0293 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(19): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAAGAAGA others(7): Show |
1 | a0001c0001t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(18): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0025g0112 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1153+1383_1153+138 others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | A | G | 2 | a0002c0002t0083g0121 a0009c0016t0001g0193 |
2 | HG03225.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1153+1384T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | AAAAG | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(52): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1153+1380_1153+138 others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | AAAAGAAA others(1): Show |
A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
29 | HG00099.hp2 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153+1376_1153+138 others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | AAAAGAAA others(5): Show |
A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(14): Show |
17 | HG00621.hp1 HG00639.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1153+1372_1153+138 others(16): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | AAAAGAAA others(9): Show |
A | 1 | a0001c0001t0016g0133 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1153+1368_1153+138 others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | AAAAGAAA others(13): Show |
A | 2 | a0001c0001t0001g0003 a0001c0001t0013g0134 |
2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1153+1364_1153+138 others(24): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256145 | AAAAGAAA others(25): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1153+1352_1153+138 others(36): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256145 | |||||||
| chr3:101256165 | GAAAGAAA others(4): Show |
G | 1 | a0002c0003t0002g0272 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1153+1353_1153+136 others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256165 | |||||||
| chr3:101256172 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1153+1357T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256172 | |||||||
| chr3:101256189 | G | GAAAGAAA others(22): Show |
1 | a0001c0001t0052g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+1311_1153+133 others(33): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256189 | |||||||
| chr3:101256193 | G | GAAAGAAA others(6): Show |
1 | a0001c0001t0051g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1153+1323_1153+133 others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256193 | |||||||
| chr3:101256208 | A | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1321T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256208 | |||||||
| chr3:101256212 | A | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1317T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256212 | |||||||
| chr3:101256216 | A | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1313T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256216 | |||||||
| chr3:101256217 | G | A | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1312C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | |||||||
| chr3:101256217 | G | GAAAGAAA others(3): Show |
1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1153+1311_1153+131 others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | |||||||
| chr3:101256217 | G | GAAAGAAA others(27): Show |
1 | a0002c0003t0058g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1153+1311_1153+131 others(38): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | |||||||
| chr3:101256217 | G | GAAAGAAA others(39): Show |
1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1153+1311_1153+131 others(50): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | |||||||
| chr3:101256217 | G | GAACGAAC others(1): Show |
4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+1311_1153+131 others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256217 | |||||||
| chr3:101256218 | A | AAAGAAAG others(4): Show |
1 | a0002c0003t0003g0232 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1153+1310_1153+131 others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256218 | |||||||
| chr3:101256218 | A | AAAGAAAG others(12): Show |
1 | a0002c0002t0009g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1153+1310_1153+131 others(23): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256218 | |||||||
| chr3:101256263 | T | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1153+1266A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256263 | |||||||
| chr3:101256449 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
229 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1153+1080G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256449 | |||||||
| chr3:101256598 | C | G | 6 | a0001c0001t0008g0217 a0001c0001t0010g0035 a0001c0001t0010g0218 others(3): Show |
7 | HG00741.hp2 HG01123.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153+931G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256598 | |||||||
| chr3:101256600 | G | C | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+929C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256600 | |||||||
| chr3:101256710 | A | T | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+819T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256710 | |||||||
| chr3:101256751 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1153+778G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256751 | |||||||
| chr3:101256753 | C | T | 2 | a0001c0001t0034g0278 a0001c0001t0034g0279 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1153+776G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256753 | |||||||
| chr3:101256988 | T | C | 1 | a0001c0001t0014g0215 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1153+541A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101256988 | |||||||
| chr3:101257033 | A | G | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153+496T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257033 | |||||||
| chr3:101257146 | A | G | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+383T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257146 | |||||||
| chr3:101257231 | A | C | 1 | a0001c0001t0034g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1153+298T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257231 | |||||||
| chr3:101257349 | G | A | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+180C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257349 | |||||||
| chr3:101257370 | A | T | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+159T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257370 | |||||||
| chr3:101257375 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
229 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1153+154G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 10/18 | chr3 | 101257375 | |||||||
| chr3:101257854 | A | G | 2 | a0002c0003t0002g0228 a0002c0003t0003g0024 |
3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.909-81T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101257854 | |||||||
| chr3:101257911 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
300 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.909-138C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101257911 | |||||||
| chr3:101257922 | A | C | 8 | a0002c0003t0058g0229 a0002c0003t0097g0227 a0003c0004t0046g0315 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-149T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101257922 | |||||||
| chr3:101258394 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
229 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.909-621A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258394 | |||||||
| chr3:101258566 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.909-793G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258566 | |||||||
| chr3:101258653 | T | C | 3 | a0001c0001t0012g0142 a0001c0001t0070g0141 a0001c0001t0078g0143 |
3 | HG01952.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.909-880A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258653 | |||||||
| chr3:101258784 | A | T | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-1011T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101258784 | |||||||
| chr3:101259063 | C | T | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.909-1290G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259063 | |||||||
| chr3:101259295 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.909-1522C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259295 | |||||||
| chr3:101259436 | C | T | 8 | a0002c0003t0058g0229 a0002c0003t0097g0227 a0003c0004t0046g0315 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-1663G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259436 | |||||||
| chr3:101259444 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
296 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.909-1671G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259444 | |||||||
| chr3:101259535 | T | C | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-1762A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259535 | |||||||
| chr3:101259598 | C | T | 37 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 others(34): Show |
39 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.909-1825G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259598 | |||||||
| chr3:101259701 | G | A | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-1928C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259701 | |||||||
| chr3:101259951 | G | C | 53 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.909-2178C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101259951 | |||||||
| chr3:101260106 | C | T | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-2333G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260106 | |||||||
| chr3:101260141 | T | C | 60 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(57): Show |
67 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.909-2368A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260141 | |||||||
| chr3:101260176 | G | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
296 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.909-2403C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260176 | |||||||
| chr3:101260301 | G | A | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2528C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260301 | |||||||
| chr3:101260412 | A | C | 89 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 others(86): Show |
96 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.909-2639T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260412 | |||||||
| chr3:101260633 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.909-2860T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260633 | |||||||
| chr3:101260681 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.909-2908G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260681 | |||||||
| chr3:101260685 | C | T | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-2912G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260685 | |||||||
| chr3:101260821 | A | G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.909-3048T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260821 | |||||||
| chr3:101260982 | A | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
229 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.909-3209T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101260982 | |||||||
| chr3:101261207 | G | A | 1 | a0002c0003t0003g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.909-3434C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261207 | |||||||
| chr3:101261292 | G | T | 1 | a0001c0001t0025g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.909-3519C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261292 | |||||||
| chr3:101261334 | A | C | 1 | a0002c0003t0002g0265 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909-3561T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261334 | |||||||
| chr3:101261393 | C | T | 10 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(7): Show |
11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.909-3620G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261393 | |||||||
| chr3:101261467 | A | G | 60 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(57): Show |
67 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.909-3694T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261467 | |||||||
| chr3:101261500 | T | G | 8 | a0002c0003t0058g0229 a0002c0003t0097g0227 a0003c0004t0046g0315 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-3727A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261500 | |||||||
| chr3:101261558 | A | G | 1 | a0001c0001t0013g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.909-3785T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261558 | |||||||
| chr3:101261697 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-3924A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261697 | |||||||
| chr3:101261800 | C | G | 1 | a0001c0001t0012g0126 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.909-4027G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261800 | |||||||
| chr3:101261802 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.909-4029T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261802 | |||||||
| chr3:101261863 | G | A | 2 | a0001c0001t0001g0276 a0002c0002t0085g0136 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.909-4090C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261863 | |||||||
| chr3:101261962 | C | T | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.909-4189G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101261962 | |||||||
| chr3:101262005 | A | G | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.909-4232T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262005 | |||||||
| chr3:101262345 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.909-4572A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262345 | |||||||
| chr3:101262389 | T | G | 1 | a0001c0001t0065g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.909-4616A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262389 | |||||||
| chr3:101262466 | T | G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.909-4693A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262466 | |||||||
| chr3:101262582 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
229 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.909-4809T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262582 | |||||||
| chr3:101262633 | AAT | A | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-4862_909-4861d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262633 | |||||||
| chr3:101262637 | A | G | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-4864T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262637 | |||||||
| chr3:101262711 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.908+4800G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262711 | |||||||
| chr3:101262770 | C | CA | 54 | a0001c0001t0001g0159 a0001c0001t0044g0178 a0002c0003t0002g0008 others(51): Show |
61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.908+4740dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262770 | |||||||
| chr3:101262770 | C | CAA | 6 | a0002c0003t0002g0267 a0002c0003t0058g0229 a0002c0003t0075g0233 others(3): Show |
6 | HG00639.hp2 HG01993.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+4739_908+4740d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262770 | |||||||
| chr3:101262770 | CA | C | 15 | a0001c0001t0008g0217 a0001c0001t0010g0035 a0001c0001t0010g0218 others(12): Show |
17 | HG01123.hp1 HG01884.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.908+4740delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262770 | |||||||
| chr3:101262784 | C | A | 11 | a0001c0001t0026g0305 a0001c0001t0026g0307 a0002c0002t0011g0291 others(8): Show |
11 | HG00280.hp2 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.908+4727G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262784 | |||||||
| chr3:101262896 | G | A | 2 | a0001c0001t0006g0128 a0001c0001t0016g0204 |
2 | NA18939.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.908+4615C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262896 | |||||||
| chr3:101262956 | G | A | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+4555C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101262956 | |||||||
| chr3:101263088 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.908+4423T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263088 | |||||||
| chr3:101263115 | C | A | 4 | a0001c0001t0007g0005 a0001c0001t0007g0106 a0001c0001t0007g0107 others(1): Show |
6 | NA18946.hp2 NA18947.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+4396G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263115 | |||||||
| chr3:101263146 | A | G | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+4365T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263146 | |||||||
| chr3:101263334 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.908+4177A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263334 | |||||||
| chr3:101263659 | C | G | 1 | a0001c0001t0063g0219 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.908+3852G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263659 | |||||||
| chr3:101263681 | A | C | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+3830T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263681 | |||||||
| chr3:101263833 | A | G | 1 | a0002c0003t0003g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.908+3678T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263833 | |||||||
| chr3:101263857 | C | CA | 7 | a0001c0001t0008g0217 a0001c0001t0010g0035 a0001c0001t0010g0218 others(4): Show |
8 | HG01123.hp1 HG01943.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+3653dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263857 | |||||||
| chr3:101263857 | CA | C | 9 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0006g0128 others(6): Show |
9 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.908+3653delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263857 | |||||||
| chr3:101263876 | G | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.908+3635C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101263876 | |||||||
| chr3:101264251 | T | C | 1 | a0001c0001t0012g0203 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.908+3260A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264251 | |||||||
| chr3:101264277 | A | C | 1 | a0011c0010t0017g0083 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.908+3234T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264277 | |||||||
| chr3:101264330 | G | A | 1 | a0001c0001t0007g0109 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.908+3181C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264330 | |||||||
| chr3:101264610 | T | C | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+2901A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264610 | |||||||
| chr3:101264969 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0029g0102 a0001c0001t0029g0103 |
4 | HG01515.hp2 HG01517.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+2542C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101264969 | |||||||
| chr3:101265208 | T | C | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.908+2303A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265208 | |||||||
| chr3:101265355 | G | A | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.908+2156C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265355 | |||||||
| chr3:101265360 | A | G | 1 | a0001c0001t0022g0110 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.908+2151T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265360 | |||||||
| chr3:101265761 | G | A | 2 | a0001c0001t0021g0104 a0001c0001t0025g0089 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.908+1750C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265761 | |||||||
| chr3:101265767 | C | T | 3 | a0001c0001t0008g0004 a0001c0001t0008g0022 a0001c0001t0008g0053 |
6 | HG00642.hp1 HG01167.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+1744G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265767 | |||||||
| chr3:101265775 | G | A | 7 | a0002c0003t0058g0229 a0003c0004t0046g0315 a0003c0004t0047g0287 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1736C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101265775 | |||||||
| chr3:101266102 | G | A | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.908+1409C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266102 | |||||||
| chr3:101266559 | T | C | 8 | a0002c0003t0058g0229 a0002c0003t0097g0227 a0003c0004t0046g0315 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.908+952A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266559 | |||||||
| chr3:101266580 | T | C | 3 | a0001c0001t0013g0040 a0001c0001t0014g0039 a0001c0001t0020g0037 |
3 | NA18957.hp2 NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.908+931A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266580 | |||||||
| chr3:101266853 | G | A | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.908+658C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266853 | |||||||
| chr3:101266863 | C | T | 1 | a0001c0001t0038g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.908+648G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101266863 | |||||||
| chr3:101267133 | A | G | 1 | a0002c0003t0002g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.908+378T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267133 | |||||||
| chr3:101267300 | T | A | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.908+211A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267300 | |||||||
| chr3:101267353 | T | C | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.908+158A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267353 | |||||||
| chr3:101267444 | A | G | 1 | a0001c0001t0056g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.908+67T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267444 | |||||||
| chr3:101267477 | T | G | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+34A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 9/18 | chr3 | 101267477 | |||||||
| chr3:101267612 | C | T | 17 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(14): Show |
18 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.888-81G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267612 | |||||||
| chr3:101267689 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.888-158C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267689 | |||||||
| chr3:101267810 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.888-279T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267810 | |||||||
| chr3:101267858 | C | CT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
219 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.888-328dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267858 | |||||||
| chr3:101267872 | A | G | 1 | a0001c0001t0068g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.888-341T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267872 | |||||||
| chr3:101267934 | G | A | 17 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(14): Show |
18 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.888-403C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267934 | |||||||
| chr3:101267968 | C | A | 4 | a0003c0004t0046g0315 a0003c0004t0047g0287 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.888-437G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101267968 | |||||||
| chr3:101268135 | T | C | 8 | a0002c0003t0002g0027 a0002c0003t0002g0255 a0002c0003t0002g0273 others(5): Show |
9 | HG00733.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.888-604A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268135 | |||||||
| chr3:101268312 | C | T | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.888-781G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268312 | |||||||
| chr3:101268415 | C | T | 5 | a0001c0001t0008g0217 a0001c0001t0010g0035 a0001c0001t0010g0218 others(2): Show |
6 | HG01123.hp1 HG01943.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-884G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268415 | |||||||
| chr3:101268620 | C | CAT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.887+893_887+894dup others(2): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268620 | |||||||
| chr3:101268620 | C | CATAT | 21 | a0001c0001t0008g0053 a0001c0001t0008g0217 a0001c0001t0010g0035 others(18): Show |
23 | HG00438.hp2 HG01123.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.887+891_887+894dup others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268620 | |||||||
| chr3:101268675 | T | C | 10 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(7): Show |
11 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.887+840A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268675 | |||||||
| chr3:101268787 | G | A | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.887+728C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268787 | |||||||
| chr3:101268937 | G | C | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.887+578C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101268937 | |||||||
| chr3:101269003 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.887+512T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269003 | |||||||
| chr3:101269134 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.887+381T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269134 | |||||||
| chr3:101269147 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.887+368G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269147 | |||||||
| chr3:101269187 | C | T | 16 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(13): Show |
17 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.887+328G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269187 | |||||||
| chr3:101269201 | C | A | 2 | a0002c0003t0002g0265 a0002c0003t0002g0266 |
2 | HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.887+314G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269201 | |||||||
| chr3:101269204 | G | A | 1 | a0002c0002t0039g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.887+311C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269204 | |||||||
| chr3:101269209 | C | CCTTCAGG | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.887+305_887+306ins others(7): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269209 | |||||||
| chr3:101269260 | G | A | 2 | a0001c0001t0023g0187 a0001c0001t0023g0195 |
2 | HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.887+255C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269260 | |||||||
| chr3:101269434 | A | G | 1 | a0001c0001t0065g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.887+81T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 8/18 | chr3 | 101269434 | |||||||
| chr3:101269785 | C | T | 16 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(13): Show |
17 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-212G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269785 | |||||||
| chr3:101269843 | G | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.829-270C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269843 | |||||||
| chr3:101269872 | T | C | 5 | a0002c0003t0002g0271 a0002c0003t0002g0272 a0002c0003t0003g0270 others(2): Show |
5 | HG00673.hp1 HG02015.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-299A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269872 | |||||||
| chr3:101269926 | C | CT | 64 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0280 others(61): Show |
70 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.829-354dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269926 | |||||||
| chr3:101269926 | CT | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0174 a0001c0001t0001g0188 others(4): Show |
8 | HG01975.hp2 HG02280.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-354delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269926 | |||||||
| chr3:101269926 | CTTTTTTT others(5): Show |
C | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829-365_829-354del others(12): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269926 | |||||||
| chr3:101269952 | A | T | 1 | a0002c0002t0017g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.829-379T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269952 | |||||||
| chr3:101269979 | G | A | 3 | a0001c0001t0066g0148 a0001c0001t0069g0149 a0001c0001t0072g0150 |
3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.829-406C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101269979 | |||||||
| chr3:101270011 | A | C | 13 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.829-438T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270011 | |||||||
| chr3:101270032 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0023g0180 a0001c0017t0001g0181 |
4 | HG02027.hp2 HG02071.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-459C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270032 | |||||||
| chr3:101270238 | A | T | 16 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(13): Show |
17 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-665T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270238 | |||||||
| chr3:101270268 | C | A | 1 | a0003c0004t0049g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829-695G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270268 | |||||||
| chr3:101270351 | A | G | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829-778T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270351 | |||||||
| chr3:101270544 | A | C | 3 | a0001c0001t0066g0148 a0001c0001t0069g0149 a0001c0001t0072g0150 |
3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.829-971T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270544 | |||||||
| chr3:101270573 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.829-1000C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270573 | |||||||
| chr3:101270633 | C | T | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.829-1060G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270633 | |||||||
| chr3:101270663 | GGTGGTGG others(9): Show |
G | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.829-1106_829-1091d others(18): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270663 | |||||||
| chr3:101270785 | C | T | 4 | a0001c0001t0037g0285 a0001c0001t0071g0282 a0001c0001t0074g0286 others(1): Show |
4 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-1212G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270785 | |||||||
| chr3:101270799 | A | T | 1 | a0001c0001t0063g0219 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.829-1226T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270799 | |||||||
| chr3:101270953 | C | T | 8 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 others(5): Show |
9 | HG00280.hp1 HG01978.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-1380G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270953 | |||||||
| chr3:101270959 | A | G | 13 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.829-1386T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270959 | |||||||
| chr3:101270997 | A | G | 3 | a0001c0001t0013g0120 a0001c0001t0013g0123 a0001c0001t0020g0122 |
3 | HG00280.hp1 HG02004.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.829-1424T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101270997 | |||||||
| chr3:101271121 | A | C | 14 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(11): Show |
15 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.829-1548T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271121 | |||||||
| chr3:101271133 | C | T | 11 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(8): Show |
12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.829-1560G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271133 | |||||||
| chr3:101271144 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.829-1571C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271144 | |||||||
| chr3:101271403 | T | C | 1 | a0001c0001t0062g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.829-1830A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271403 | |||||||
| chr3:101271419 | G | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.829-1846C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271419 | |||||||
| chr3:101271630 | G | C | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1951C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271630 | |||||||
| chr3:101271920 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1661C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101271920 | |||||||
| chr3:101272050 | C | A | 11 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(8): Show |
12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.828+1531G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272050 | |||||||
| chr3:101272055 | T | C | 1 | a0001c0001t0008g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.828+1526A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272055 | |||||||
| chr3:101272099 | G | GCA | 5 | a0002c0002t0039g0312 a0002c0002t0084g0310 a0002c0002t0086g0311 others(2): Show |
5 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+1480_828+1481d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272099 | |||||||
| chr3:101272099 | GCA | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.828+1480_828+1481d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272099 | |||||||
| chr3:101272116 | C | T | 1 | a0003c0004t0049g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.828+1465G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272116 | |||||||
| chr3:101272118 | C | T | 2 | a0003c0004t0046g0315 a0003c0004t0048g0313 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1463G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272118 | |||||||
| chr3:101272122 | T | C | 2 | a0003c0004t0046g0315 a0003c0004t0048g0313 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+1459A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272122 | |||||||
| chr3:101272312 | G | C | 1 | a0001c0001t0052g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.828+1269C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272312 | |||||||
| chr3:101272330 | G | A | 14 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(11): Show |
15 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.828+1251C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272330 | |||||||
| chr3:101272591 | C | G | 1 | a0007c0011t0004g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.828+990G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272591 | |||||||
| chr3:101272696 | T | C | 11 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(8): Show |
12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.828+885A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272696 | |||||||
| chr3:101272702 | G | T | 92 | a0001c0001t0001g0131 a0001c0001t0001g0280 a0001c0001t0001g0281 others(89): Show |
99 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.828+879C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272702 | |||||||
| chr3:101272870 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+711C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101272870 | |||||||
| chr3:101273259 | G | A | 3 | a0001c0001t0012g0203 a0001c0001t0013g0134 a0001c0001t0016g0133 |
3 | HG02080.hp2 NA18954.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.828+322C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273259 | |||||||
| chr3:101273299 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.828+282T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273299 | |||||||
| chr3:101273311 | T | C | 1 | a0002c0002t0043g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.828+270A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273311 | |||||||
| chr3:101273541 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.828+40G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273541 | |||||||
| chr3:101273563 | T | TG | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.828+17_828+18insC | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273563 | |||||||
| chr3:101273564 | T | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.828+17A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 7/18 | chr3 | 101273564 | |||||||
| chr3:101273922 | G | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667-180C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101273922 | |||||||
| chr3:101273923 | A | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667-181T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101273923 | |||||||
| chr3:101274218 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.667-476T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274218 | |||||||
| chr3:101274309 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.667-567C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274309 | |||||||
| chr3:101274480 | C | T | 15 | a0001c0001t0001g0167 a0001c0001t0026g0304 a0001c0001t0026g0305 others(12): Show |
16 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.667-738G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274480 | |||||||
| chr3:101274626 | C | T | 14 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(11): Show |
15 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-884G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274626 | |||||||
| chr3:101274666 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.667-924C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274666 | |||||||
| chr3:101274689 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.667-947G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274689 | |||||||
| chr3:101274776 | G | A | 3 | a0001c0001t0016g0211 a0001c0001t0022g0137 a0001c0001t0061g0153 |
3 | NA18959.hp1 NA19066.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.666+887C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274776 | |||||||
| chr3:101274854 | G | A | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.666+809C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101274854 | |||||||
| chr3:101275063 | TA | T | 22 | a0001c0001t0010g0234 a0001c0001t0012g0203 a0001c0001t0026g0304 others(19): Show |
23 | HG00639.hp2 HG02055.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.666+599delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275063 | |||||||
| chr3:101275207 | C | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.666+456G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275207 | |||||||
| chr3:101275269 | A | G | 1 | a0001c0001t0025g0112 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.666+394T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275269 | |||||||
| chr3:101275341 | A | G | 11 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(8): Show |
12 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.666+322T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275341 | |||||||
| chr3:101275476 | G | A | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666+187C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275476 | |||||||
| chr3:101275504 | T | A | 1 | a0001c0001t0044g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.666+159A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275504 | |||||||
| chr3:101275533 | T | C | 53 | a0001c0001t0037g0284 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.666+130A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275533 | |||||||
| chr3:101275653 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.666+10G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 6/18 | chr3 | 101275653 | |||||||
| chr3:101275802 | C | T | 1 | a0002c0002t0017g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.584-57G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101275802 | |||||||
| chr3:101275837 | T | G | 1 | a0001c0001t0007g0107 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.584-92A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101275837 | |||||||
| chr3:101275873 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.584-128G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101275873 | |||||||
| chr3:101276104 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.584-359A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276104 | |||||||
| chr3:101276320 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.583+344C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276320 | |||||||
| chr3:101276323 | C | T | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.583+341G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276323 | |||||||
| chr3:101276356 | C | T | 1 | a0001c0001t0020g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.583+308G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 5/18 | chr3 | 101276356 | |||||||
| chr3:101276858 | T | A | 1 | a0001c0001t0055g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.534-145A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101276858 | |||||||
| chr3:101276927 | T | C | 1 | a0001c0001t0010g0035 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.534-214A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101276927 | |||||||
| chr3:101277170 | G | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-457C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277170 | |||||||
| chr3:101277251 | G | T | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.534-538C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277251 | |||||||
| chr3:101277310 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.534-597A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277310 | |||||||
| chr3:101277467 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-754G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277467 | |||||||
| chr3:101277469 | A | T | 1 | a0002c0002t0082g0299 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.534-756T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277469 | |||||||
| chr3:101277567 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.534-854A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277567 | |||||||
| chr3:101277728 | A | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-1015T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277728 | |||||||
| chr3:101277785 | T | C | 1 | a0002c0003t0002g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.534-1072A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277785 | |||||||
| chr3:101277826 | T | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-1113A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277826 | |||||||
| chr3:101277953 | A | G | 2 | a0002c0003t0002g0228 a0002c0003t0003g0024 |
3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.534-1240T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101277953 | |||||||
| chr3:101278001 | CA | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-1289delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278001 | |||||||
| chr3:101278061 | C | T | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-1348G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278061 | |||||||
| chr3:101278327 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-1614C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278327 | |||||||
| chr3:101278331 | C | G | 3 | a0001c0001t0012g0142 a0001c0001t0070g0141 a0001c0001t0078g0143 |
3 | HG01952.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.534-1618G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278331 | |||||||
| chr3:101278378 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.534-1665A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278378 | |||||||
| chr3:101278452 | T | G | 3 | a0001c0001t0066g0148 a0001c0001t0069g0149 a0001c0001t0072g0150 |
3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.534-1739A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278452 | |||||||
| chr3:101278713 | AC | A | 4 | a0001c0001t0044g0178 a0003c0004t0046g0315 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2001delG | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278713 | |||||||
| chr3:101278714 | C | A | 1 | a0001c0001t0001g0007 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.534-2001G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278714 | |||||||
| chr3:101278902 | A | T | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2189T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278902 | |||||||
| chr3:101278937 | T | C | 1 | a0002c0002t0028g0076 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.534-2224A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278937 | |||||||
| chr3:101278970 | G | C | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-2257C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101278970 | |||||||
| chr3:101279026 | A | T | 2 | a0002c0002t0009g0045 a0002c0002t0009g0066 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.534-2313T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279026 | |||||||
| chr3:101279088 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-2375G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279088 | |||||||
| chr3:101279158 | TA | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-2446delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279158 | |||||||
| chr3:101279388 | A | C | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2675T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279388 | |||||||
| chr3:101279417 | A | T | 3 | a0001c0001t0012g0214 a0001c0001t0013g0093 a0001c0001t0025g0112 |
3 | HG02040.hp2 HG02071.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.534-2704T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279417 | |||||||
| chr3:101279569 | T | C | 15 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(12): Show |
16 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-2856A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279569 | |||||||
| chr3:101279888 | C | T | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-3175G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101279888 | |||||||
| chr3:101280018 | T | C | 4 | a0002c0002t0028g0147 a0003c0004t0046g0315 a0003c0004t0048g0313 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-3305A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280018 | |||||||
| chr3:101280207 | C | A | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.534-3494G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280207 | |||||||
| chr3:101280331 | G | A | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-3618C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280331 | |||||||
| chr3:101280498 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-3785C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280498 | |||||||
| chr3:101280823 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.534-4110G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280823 | |||||||
| chr3:101280825 | T | C | 88 | a0001c0001t0001g0131 a0001c0001t0006g0010 a0001c0001t0006g0032 others(85): Show |
95 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.534-4112A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280825 | |||||||
| chr3:101280872 | G | A | 38 | a0001c0001t0065g0154 a0002c0002t0004g0013 a0002c0002t0004g0063 others(35): Show |
39 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.534-4159C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280872 | |||||||
| chr3:101280930 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-4217G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280930 | |||||||
| chr3:101280936 | G | A | 1 | a0001c0001t0055g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.534-4223C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280936 | |||||||
| chr3:101280946 | CA | C | 49 | a0001c0001t0036g0041 a0001c0001t0036g0043 a0001c0001t0065g0154 others(46): Show |
51 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.534-4234delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280946 | |||||||
| chr3:101280956 | A | C | 15 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(12): Show |
16 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-4243T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280956 | |||||||
| chr3:101280987 | TATTCTCA others(6): Show |
T | 1 | a0002c0002t0082g0299 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.534-4287_534-4275d others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280987 | |||||||
| chr3:101280995 | A | G | 52 | a0002c0003t0002g0008 a0002c0003t0002g0027 a0002c0003t0002g0228 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.534-4282T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101280995 | |||||||
| chr3:101281179 | G | T | 2 | a0002c0002t0009g0292 a0002c0002t0027g0293 |
2 | HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.534-4466C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281179 | |||||||
| chr3:101281445 | G | A | 1 | a0001c0001t0007g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.534-4732C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281445 | |||||||
| chr3:101281470 | T | C | 15 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(12): Show |
16 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-4757A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281470 | |||||||
| chr3:101281621 | G | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0164 others(3): Show |
8 | NA18939.hp1 NA18941.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-4908C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281621 | |||||||
| chr3:101281633 | T | A | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.534-4920A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281633 | |||||||
| chr3:101281789 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-5076C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281789 | |||||||
| chr3:101281811 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-5098C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281811 | |||||||
| chr3:101281812 | C | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-5099G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101281812 | |||||||
| chr3:101282082 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534-5369T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282082 | |||||||
| chr3:101282107 | T | G | 12 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.534-5394A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282107 | |||||||
| chr3:101282122 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.534-5409A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282122 | |||||||
| chr3:101282123 | G | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.534-5410C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282123 | |||||||
| chr3:101282130 | A | G | 1 | a0002c0002t0017g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.534-5417T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282130 | |||||||
| chr3:101282220 | G | A | 1 | a0001c0001t0023g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.534-5507C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282220 | |||||||
| chr3:101282259 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-5546C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282259 | |||||||
| chr3:101282333 | T | C | 18 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(15): Show |
19 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.534-5620A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282333 | |||||||
| chr3:101282604 | C | A | 1 | a0002c0002t0011g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.534-5891G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282604 | |||||||
| chr3:101282638 | T | C | 4 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(1): Show |
5 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-5925A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282638 | |||||||
| chr3:101282748 | T | C | 1 | a0002c0003t0024g0269 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.534-6035A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282748 | |||||||
| chr3:101282836 | G | T | 1 | a0002c0003t0003g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.534-6123C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282836 | |||||||
| chr3:101282913 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.534-6200C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282913 | |||||||
| chr3:101282915 | A | G | 53 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.534-6202T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101282915 | |||||||
| chr3:101283018 | T | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.534-6305A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283018 | |||||||
| chr3:101283092 | G | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-6379C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283092 | |||||||
| chr3:101283171 | C | T | 1 | a0002c0002t0083g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.534-6458G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283171 | |||||||
| chr3:101283179 | T | G | 1 | a0002c0003t0002g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.534-6466A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283179 | |||||||
| chr3:101283213 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0179 others(2): Show |
8 | HG02027.hp2 HG02071.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-6500G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283213 | |||||||
| chr3:101283317 | T | C | 18 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(15): Show |
19 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.534-6604A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283317 | |||||||
| chr3:101283453 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.534-6740A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283453 | |||||||
| chr3:101283520 | C | T | 3 | a0002c0002t0039g0312 a0002c0002t0084g0310 a0002c0002t0086g0311 |
3 | HG03486.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.534-6807G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283520 | |||||||
| chr3:101283699 | C | T | 22 | a0002c0003t0002g0008 a0002c0003t0002g0238 a0002c0003t0002g0241 others(19): Show |
26 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.534-6986G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283699 | |||||||
| chr3:101283895 | TA | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
152 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.534-7183delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101283895 | |||||||
| chr3:101284198 | G | A | 1 | a0002c0002t0091g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.533+7281C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284198 | |||||||
| chr3:101284220 | A | G | 1 | a0002c0003t0075g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.533+7259T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284220 | |||||||
| chr3:101284379 | A | G | 1 | a0002c0003t0002g0237 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.533+7100T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284379 | |||||||
| chr3:101284565 | C | CA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.533+6913dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284565 | |||||||
| chr3:101284565 | C | CAA | 15 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0164 others(12): Show |
18 | HG01884.hp2 HG01975.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.533+6912_533+6913d others(4): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284565 | |||||||
| chr3:101284771 | T | C | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.533+6708A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101284771 | |||||||
| chr3:101285065 | A | G | 1 | a0001c0001t0044g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.533+6414T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285065 | |||||||
| chr3:101285336 | G | A | 53 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.533+6143C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285336 | |||||||
| chr3:101285491 | C | A | 1 | a0002c0003t0002g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.533+5988G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285491 | |||||||
| chr3:101285524 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533+5955T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285524 | |||||||
| chr3:101285538 | T | C | 4 | a0001c0001t0007g0005 a0001c0001t0007g0106 a0001c0001t0007g0107 others(1): Show |
6 | NA18946.hp2 NA18947.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.533+5941A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285538 | |||||||
| chr3:101285575 | G | A | 1 | a0001c0001t0007g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.533+5904C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285575 | |||||||
| chr3:101285628 | T | C | 14 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(11): Show |
15 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.533+5851A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285628 | |||||||
| chr3:101285711 | G | C | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0022g0110 others(2): Show |
5 | HG00621.hp1 NA18948.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+5768C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285711 | |||||||
| chr3:101285828 | T | G | 2 | a0001c0001t0001g0276 a0002c0002t0085g0136 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.533+5651A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285828 | |||||||
| chr3:101285964 | C | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.533+5515G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285964 | |||||||
| chr3:101285975 | A | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+5504T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101285975 | |||||||
| chr3:101286091 | TCCTTCTC others(4): Show |
T | 1 | a0001c0001t0001g0221 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.533+5377_533+5387d others(13): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286091 | |||||||
| chr3:101286263 | A | C | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0212 others(2): Show |
5 | HG01074.hp1 HG01978.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+5216T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286263 | |||||||
| chr3:101286346 | A | G | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+5133T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286346 | |||||||
| chr3:101286394 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+5085G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286394 | |||||||
| chr3:101286424 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+5055A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286424 | |||||||
| chr3:101286516 | T | C | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.533+4963A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286516 | |||||||
| chr3:101286659 | G | A | 1 | a0001c0001t0044g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.533+4820C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286659 | |||||||
| chr3:101286703 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+4776G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286703 | |||||||
| chr3:101286937 | C | T | 1 | a0002c0003t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.533+4542G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101286937 | |||||||
| chr3:101287277 | G | T | 1 | a0001c0001t0025g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533+4202C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287277 | |||||||
| chr3:101287281 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.533+4198C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287281 | |||||||
| chr3:101287309 | T | C | 1 | a0002c0002t0017g0078 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.533+4170A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287309 | |||||||
| chr3:101287360 | T | G | 1 | a0003c0004t0049g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.533+4119A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287360 | |||||||
| chr3:101287655 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+3824T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287655 | |||||||
| chr3:101287725 | T | C | 1 | a0001c0001t0025g0112 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.533+3754A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287725 | |||||||
| chr3:101287740 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533+3739A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287740 | |||||||
| chr3:101287793 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+3686T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101287793 | |||||||
| chr3:101288034 | C | T | 1 | a0001c0001t0021g0090 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.533+3445G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288034 | |||||||
| chr3:101288043 | C | A | 1 | a0002c0002t0009g0079 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.533+3436G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288043 | |||||||
| chr3:101288315 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0196 others(1): Show |
4 | HG01175.hp1 HG01256.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+3164C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288315 | |||||||
| chr3:101288400 | T | A | 1 | a0001c0001t0055g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.533+3079A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288400 | |||||||
| chr3:101288705 | C | T | 2 | a0001c0001t0037g0285 a0001c0001t0071g0282 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.533+2774G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288705 | |||||||
| chr3:101288706 | G | A | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533+2773C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288706 | |||||||
| chr3:101288976 | T | A | 1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+2503A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101288976 | |||||||
| chr3:101290027 | C | T | 1 | a0001c0001t0013g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.533+1452G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290027 | |||||||
| chr3:101290034 | G | A | 1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+1445C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290034 | |||||||
| chr3:101290064 | A | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+1415T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290064 | |||||||
| chr3:101290065 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+1414A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290065 | |||||||
| chr3:101290127 | G | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.533+1352C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290127 | |||||||
| chr3:101290163 | A | T | 3 | a0002c0002t0004g0063 a0002c0002t0015g0050 a0002c0002t0027g0064 |
3 | NA18947.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.533+1316T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290163 | |||||||
| chr3:101290221 | G | A | 1 | a0001c0001t0010g0116 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.533+1258C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290221 | |||||||
| chr3:101290277 | C | T | 1 | a0001c0001t0025g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533+1202G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290277 | |||||||
| chr3:101290278 | G | A | 1 | a0002c0003t0002g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.533+1201C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290278 | |||||||
| chr3:101290327 | C | T | 1 | a0002c0003t0003g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.533+1152G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290327 | |||||||
| chr3:101290480 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.533+999C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290480 | |||||||
| chr3:101290487 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.533+992G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290487 | |||||||
| chr3:101290783 | T | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533+696A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290783 | |||||||
| chr3:101290915 | T | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.533+564A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290915 | |||||||
| chr3:101290955 | T | C | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.533+524A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290955 | |||||||
| chr3:101290963 | T | A | 4 | a0001c0001t0066g0148 a0001c0001t0069g0149 a0001c0001t0072g0150 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+516A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101290963 | |||||||
| chr3:101291023 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.533+456G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291023 | |||||||
| chr3:101291207 | T | C | 1 | a0002c0003t0058g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.533+272A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291207 | |||||||
| chr3:101291281 | G | A | 1 | a0001c0001t0022g0137 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.533+198C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291281 | |||||||
| chr3:101291299 | T | C | 3 | a0002c0003t0002g0259 a0002c0003t0003g0232 a0002c0003t0059g0260 |
3 | NA18955.hp1 NA18969.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.533+180A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291299 | |||||||
| chr3:101291370 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0165 |
5 | HG02738.hp2 HG03704.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+109C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291370 | |||||||
| chr3:101291413 | G | A | 1 | a0001c0001t0010g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.533+66C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 4/18 | chr3 | 101291413 | |||||||
| chr3:101291655 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.502-145C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101291655 | |||||||
| chr3:101291834 | C | A | 1 | a0001c0001t0022g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.502-324G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101291834 | |||||||
| chr3:101291988 | G | A | 1 | a0001c0001t0044g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502-478C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101291988 | |||||||
| chr3:101292001 | C | A | 1 | a0003c0009t0050g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.502-491G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292001 | |||||||
| chr3:101292019 | C | T | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-509G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292019 | |||||||
| chr3:101292022 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.502-512G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292022 | |||||||
| chr3:101292166 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(49): Show |
73 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.502-656A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292166 | |||||||
| chr3:101292279 | G | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0163 others(3): Show |
11 | NA18747.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-769C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292279 | |||||||
| chr3:101292339 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.502-829G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292339 | |||||||
| chr3:101292585 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0164 others(2): Show |
7 | NA18939.hp1 NA18941.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-1075T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292585 | |||||||
| chr3:101292658 | C | T | 1 | a0001c0001t0056g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.502-1148G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292658 | |||||||
| chr3:101292660 | C | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-1150G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292660 | |||||||
| chr3:101292661 | C | G | 1 | a0001c0001t0052g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.502-1151G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292661 | |||||||
| chr3:101292693 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(65): Show |
93 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.502-1183G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292693 | |||||||
| chr3:101292780 | T | C | 1 | a0002c0003t0003g0261 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.502-1270A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292780 | |||||||
| chr3:101292841 | A | C | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502-1331T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292841 | |||||||
| chr3:101292842 | T | C | 1 | a0002c0003t0002g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.502-1332A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292842 | |||||||
| chr3:101292896 | A | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0157 a0001c0001t0001g0168 others(4): Show |
8 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-1386T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292896 | |||||||
| chr3:101292973 | G | A | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-1463C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101292973 | |||||||
| chr3:101293067 | G | A | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.502-1557C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293067 | |||||||
| chr3:101293262 | C | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-1752G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293262 | |||||||
| chr3:101293490 | A | G | 2 | a0001c0001t0012g0119 a0001c0001t0014g0215 |
2 | HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.502-1980T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293490 | |||||||
| chr3:101293506 | TA | T | 4 | a0002c0002t0011g0009 a0002c0002t0011g0291 a0002c0002t0015g0294 others(1): Show |
6 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-1997delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293506 | |||||||
| chr3:101293535 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-2025G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293535 | |||||||
| chr3:101293542 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-2032T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293542 | |||||||
| chr3:101293623 | C | T | 2 | a0002c0002t0009g0292 a0002c0002t0027g0293 |
2 | HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.502-2113G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293623 | |||||||
| chr3:101293692 | A | G | 1 | a0002c0002t0004g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.502-2182T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293692 | |||||||
| chr3:101293823 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-2313T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293823 | |||||||
| chr3:101293979 | G | A | 1 | a0001c0001t0081g0138 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.502-2469C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293979 | |||||||
| chr3:101293987 | A | T | 1 | a0002c0003t0002g0008 | 3 | NA18979.hp1 NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.502-2477T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101293987 | |||||||
| chr3:101294037 | A | G | 1 | a0001c0001t0012g0203 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.502-2527T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294037 | |||||||
| chr3:101294138 | G | A | 1 | a0002c0002t0043g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.502-2628C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294138 | |||||||
| chr3:101294156 | T | C | 3 | a0001c0001t0012g0142 a0001c0001t0070g0141 a0001c0001t0078g0143 |
3 | HG01952.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.502-2646A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294156 | |||||||
| chr3:101294610 | T | C | 1 | a0001c0001t0055g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.502-3100A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294610 | |||||||
| chr3:101294754 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.502-3244T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294754 | |||||||
| chr3:101294854 | CT | C | 6 | a0001c0001t0020g0114 a0002c0002t0009g0082 a0002c0002t0015g0198 others(3): Show |
6 | NA18747.hp1 NA18945.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-3345delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294854 | |||||||
| chr3:101294863 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-3353T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294863 | |||||||
| chr3:101294935 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.502-3425C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294935 | |||||||
| chr3:101294956 | G | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-3446C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101294956 | |||||||
| chr3:101295137 | G | T | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502-3627C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295137 | |||||||
| chr3:101295178 | G | C | 1 | a0011c0010t0017g0083 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.502-3668C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295178 | |||||||
| chr3:101295271 | G | A | 1 | a0001c0001t0077g0061 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.502-3761C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295271 | |||||||
| chr3:101295460 | G | A | 1 | a0001c0001t0065g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.502-3950C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295460 | |||||||
| chr3:101295528 | T | C | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.502-4018A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295528 | |||||||
| chr3:101295659 | AT | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0034 others(3): Show |
9 | HG02559.hp2 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.502-4150delA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295659 | |||||||
| chr3:101295738 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-4228T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295738 | |||||||
| chr3:101295965 | A | G | 4 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(1): Show |
5 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4455T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101295965 | |||||||
| chr3:101296110 | G | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.502-4600C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296110 | |||||||
| chr3:101296169 | G | A | 1 | a0001c0001t0010g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502-4659C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296169 | |||||||
| chr3:101296261 | T | A | 1 | a0002c0003t0005g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.502-4751A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296261 | |||||||
| chr3:101296268 | C | A | 4 | a0002c0003t0018g0014 a0002c0003t0018g0084 a0002c0003t0018g0085 others(1): Show |
5 | HG01975.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4758G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296268 | |||||||
| chr3:101296698 | A | AT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-5189dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296698 | |||||||
| chr3:101296709 | G | T | 1 | a0002c0002t0004g0063 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.502-5199C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296709 | |||||||
| chr3:101296711 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-5201A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101296711 | |||||||
| chr3:101297048 | G | A | 1 | a0002c0003t0002g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.502-5538C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297048 | |||||||
| chr3:101297053 | G | C | 53 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.502-5543C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297053 | |||||||
| chr3:101297054 | C | T | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-5544G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297054 | |||||||
| chr3:101297119 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.502-5609C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297119 | |||||||
| chr3:101297151 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.502-5641C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297151 | |||||||
| chr3:101297296 | A | G | 1 | a0002c0002t0041g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502-5786T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297296 | |||||||
| chr3:101297453 | G | C | 3 | a0001c0001t0037g0285 a0001c0001t0071g0282 a0001c0001t0074g0286 |
3 | HG02055.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.502-5943C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297453 | |||||||
| chr3:101297546 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.502-6036T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297546 | |||||||
| chr3:101297585 | T | G | 1 | a0002c0002t0089g0309 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.502-6075A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297585 | |||||||
| chr3:101297724 | A | G | 54 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(51): Show |
61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.502-6214T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297724 | |||||||
| chr3:101297990 | C | G | 1 | a0002c0002t0027g0197 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.501+6156G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101297990 | |||||||
| chr3:101298059 | T | G | 1 | a0001c0001t0008g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.501+6087A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298059 | |||||||
| chr3:101298080 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+6066A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298080 | |||||||
| chr3:101298229 | T | C | 1 | a0001c0001t0012g0202 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.501+5917A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298229 | |||||||
| chr3:101298320 | A | G | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0212 others(2): Show |
5 | HG01074.hp1 HG01978.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+5826T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298320 | |||||||
| chr3:101298356 | CCTGT | C | 4 | a0001c0001t0066g0148 a0001c0001t0069g0149 a0001c0001t0072g0150 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+5786_501+5789d others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298356 | |||||||
| chr3:101298385 | A | G | 4 | a0001c0001t0012g0142 a0001c0001t0070g0141 a0001c0001t0073g0140 others(1): Show |
4 | HG01952.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+5761T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298385 | |||||||
| chr3:101298409 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+5737T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298409 | |||||||
| chr3:101298774 | T | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.501+5372A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298774 | |||||||
| chr3:101298803 | C | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+5343G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298803 | |||||||
| chr3:101298939 | T | C | 3 | a0001c0001t0036g0041 a0001c0001t0036g0043 a0008c0015t0076g0042 |
3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.501+5207A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101298939 | |||||||
| chr3:101299389 | C | T | 1 | a0001c0001t0023g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.501+4757G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299389 | |||||||
| chr3:101299486 | G | A | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+4660C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299486 | |||||||
| chr3:101299542 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+4604T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299542 | |||||||
| chr3:101299570 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.501+4576T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299570 | |||||||
| chr3:101299584 | A | AT | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.501+4561dupA | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299584 | |||||||
| chr3:101299620 | G | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.501+4526C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299620 | |||||||
| chr3:101299643 | G | A | 2 | a0001c0001t0010g0116 a0001c0001t0016g0115 |
2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.501+4503C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101299643 | |||||||
| chr3:101300142 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.501+4004C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300142 | |||||||
| chr3:101300143 | G | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.501+4003C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300143 | |||||||
| chr3:101300307 | C | G | 1 | a0001c0001t0036g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.501+3839G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300307 | |||||||
| chr3:101300408 | C | G | 1 | a0001c0001t0001g0023 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.501+3738G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300408 | |||||||
| chr3:101300418 | G | A | 1 | a0012c0018t0005g0235 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.501+3728C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300418 | |||||||
| chr3:101300423 | C | T | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.501+3723G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300423 | |||||||
| chr3:101300550 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.501+3596A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300550 | |||||||
| chr3:101300564 | T | C | 1 | a0014c0019t0021g0117 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.501+3582A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300564 | |||||||
| chr3:101300567 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.501+3579G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300567 | |||||||
| chr3:101300752 | T | G | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.501+3394A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300752 | |||||||
| chr3:101300924 | A | T | 12 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+3222T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101300924 | |||||||
| chr3:101301002 | T | C | 1 | a0001c0001t0014g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.501+3144A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301002 | |||||||
| chr3:101301003 | C | T | 1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.501+3143G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301003 | |||||||
| chr3:101301196 | T | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.501+2950A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301196 | |||||||
| chr3:101301376 | C | A | 1 | a0002c0002t0092g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.501+2770G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301376 | |||||||
| chr3:101301623 | T | C | 1 | a0002c0002t0093g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501+2523A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301623 | |||||||
| chr3:101301649 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.501+2497G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301649 | |||||||
| chr3:101301916 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.501+2230A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101301916 | |||||||
| chr3:101302033 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.501+2113T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302033 | |||||||
| chr3:101302193 | T | C | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+1953A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302193 | |||||||
| chr3:101302229 | A | T | 1 | a0001c0001t0001g0019 | 2 | NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.501+1917T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302229 | |||||||
| chr3:101302311 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.501+1835T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302311 | |||||||
| chr3:101302346 | G | T | 1 | a0001c0001t0010g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.501+1800C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302346 | |||||||
| chr3:101302746 | T | C | 1 | a0002c0002t0004g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.501+1400A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302746 | |||||||
| chr3:101302755 | G | A | 91 | a0001c0001t0001g0131 a0001c0001t0006g0010 a0001c0001t0006g0032 others(88): Show |
98 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.501+1391C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302755 | |||||||
| chr3:101302803 | A | G | 54 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(51): Show |
61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.501+1343T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302803 | |||||||
| chr3:101302882 | C | T | 3 | a0001c0001t0033g0052 a0001c0001t0033g0158 a0001c0001t0064g0118 |
3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.501+1264G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302882 | |||||||
| chr3:101302926 | G | A | 5 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(2): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+1220C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101302926 | |||||||
| chr3:101303021 | A | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.501+1125T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303021 | |||||||
| chr3:101303134 | G | C | 40 | a0001c0001t0001g0131 a0001c0001t0006g0010 a0001c0001t0006g0032 others(37): Show |
42 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.501+1012C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303134 | |||||||
| chr3:101303164 | T | A | 4 | a0001c0001t0012g0142 a0001c0001t0070g0141 a0001c0001t0073g0140 others(1): Show |
4 | HG01952.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+982A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303164 | |||||||
| chr3:101303203 | T | C | 1 | a0002c0002t0004g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.501+943A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303203 | |||||||
| chr3:101303346 | T | C | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.501+800A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303346 | |||||||
| chr3:101303397 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.501+749C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303397 | |||||||
| chr3:101303408 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.501+738C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303408 | |||||||
| chr3:101303536 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0034 others(3): Show |
9 | HG02559.hp2 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.501+610G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303536 | |||||||
| chr3:101303546 | G | A | 1 | a0002c0002t0039g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.501+600C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303546 | |||||||
| chr3:101303828 | T | G | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.501+318A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303828 | |||||||
| chr3:101303835 | C | A | 1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.501+311G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303835 | |||||||
| chr3:101303972 | G | A | 5 | a0002c0002t0039g0312 a0002c0002t0084g0310 a0002c0002t0086g0311 others(2): Show |
5 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+174C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101303972 | |||||||
| chr3:101304032 | T | C | 54 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(51): Show |
61 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.501+114A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 3/18 | chr3 | 101304032 | |||||||
| chr3:101304584 | A | G | 3 | a0001c0001t0051g0226 a0001c0001t0052g0225 a0002c0003t0097g0227 |
3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.335-272T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304584 | |||||||
| chr3:101304627 | T | C | 1 | a0001c0001t0023g0195 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.335-315A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304627 | |||||||
| chr3:101304722 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.335-410G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304722 | |||||||
| chr3:101304739 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.335-427T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304739 | |||||||
| chr3:101304855 | T | TA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.335-544dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304855 | |||||||
| chr3:101304895 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.335-583G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304895 | |||||||
| chr3:101304904 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
101 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.335-592T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101304904 | |||||||
| chr3:101305001 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.335-689G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305001 | |||||||
| chr3:101305037 | C | T | 1 | a0001c0001t0060g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.335-725G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305037 | |||||||
| chr3:101305273 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.335-961A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305273 | |||||||
| chr3:101305303 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.335-991T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305303 | |||||||
| chr3:101305373 | G | A | 1 | a0002c0002t0039g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.335-1061C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305373 | |||||||
| chr3:101305407 | T | C | 1 | a0001c0001t0065g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.335-1095A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305407 | |||||||
| chr3:101305436 | A | G | 1 | a0012c0018t0005g0235 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.335-1124T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305436 | |||||||
| chr3:101305502 | C | T | 2 | a0003c0004t0048g0313 a0003c0004t0049g0314 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.335-1190G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305502 | |||||||
| chr3:101305677 | A | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.335-1365T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305677 | |||||||
| chr3:101305680 | A | T | 1 | a0002c0002t0011g0291 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.335-1368T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305680 | |||||||
| chr3:101305738 | A | G | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-1426T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305738 | |||||||
| chr3:101305888 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.335-1576C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305888 | |||||||
| chr3:101305965 | A | C | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.335-1653T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101305965 | |||||||
| chr3:101306240 | G | A | 3 | a0001c0001t0051g0226 a0001c0001t0052g0225 a0002c0003t0097g0227 |
3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.335-1928C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306240 | |||||||
| chr3:101306360 | G | A | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-2048C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306360 | |||||||
| chr3:101306376 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-2064T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306376 | |||||||
| chr3:101306765 | G | T | 1 | a0001c0001t0006g0033 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.335-2453C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306765 | |||||||
| chr3:101306821 | G | C | 3 | a0001c0001t0066g0148 a0001c0001t0069g0149 a0001c0001t0072g0150 |
3 | HG01884.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.335-2509C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306821 | |||||||
| chr3:101306876 | A | G | 1 | a0002c0003t0075g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.335-2564T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101306876 | |||||||
| chr3:101307093 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.335-2781A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307093 | |||||||
| chr3:101307095 | C | G | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-2783G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307095 | |||||||
| chr3:101307110 | G | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0205 others(5): Show |
10 | HG01255.hp1 HG01358.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.335-2798C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307110 | |||||||
| chr3:101307466 | C | T | 1 | a0002c0003t0024g0269 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.335-3154G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307466 | |||||||
| chr3:101307475 | A | G | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-3163T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307475 | |||||||
| chr3:101307510 | T | G | 3 | a0002c0002t0039g0312 a0002c0002t0084g0310 a0002c0002t0086g0311 |
3 | HG03486.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.335-3198A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307510 | |||||||
| chr3:101307757 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-3445A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307757 | |||||||
| chr3:101307913 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.335-3601G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307913 | |||||||
| chr3:101307928 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.335-3616G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307928 | |||||||
| chr3:101307955 | C | A | 3 | a0002c0003t0002g0265 a0002c0003t0002g0266 a0002c0003t0002g0267 |
3 | HG01081.hp2 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.335-3643G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101307955 | |||||||
| chr3:101308079 | C | T | 8 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-3767G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308079 | |||||||
| chr3:101308161 | G | A | 2 | a0001c0001t0033g0052 a0001c0001t0033g0158 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.335-3849C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308161 | |||||||
| chr3:101308244 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.335-3932A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308244 | |||||||
| chr3:101308249 | C | T | 3 | a0001c0001t0034g0278 a0001c0001t0034g0279 a0001c0001t0068g0277 |
3 | HG02280.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.335-3937G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308249 | |||||||
| chr3:101308449 | G | C | 1 | a0001c0001t0010g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.335-4137C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308449 | |||||||
| chr3:101308664 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0162 |
2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.335-4352G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308664 | |||||||
| chr3:101308682 | A | C | 1 | a0001c0001t0008g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.335-4370T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308682 | |||||||
| chr3:101308710 | T | A | 1 | a0001c0001t0001g0021 | 2 | NA18939.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.335-4398A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308710 | |||||||
| chr3:101308751 | C | T | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-4439G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308751 | |||||||
| chr3:101308915 | T | C | 1 | a0003c0014t0045g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.335-4603A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101308915 | |||||||
| chr3:101309073 | G | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-4761C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309073 | |||||||
| chr3:101309277 | T | G | 1 | a0002c0003t0024g0268 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.335-4965A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309277 | |||||||
| chr3:101309457 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-5145T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309457 | |||||||
| chr3:101309666 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.335-5354C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309666 | |||||||
| chr3:101309748 | T | C | 1 | a0002c0002t0011g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.335-5436A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309748 | |||||||
| chr3:101309871 | A | G | 1 | a0001c0001t0065g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.335-5559T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309871 | |||||||
| chr3:101309911 | A | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0162 |
2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.335-5599T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309911 | |||||||
| chr3:101309999 | G | A | 8 | a0001c0001t0037g0284 a0001c0001t0037g0285 a0001c0001t0071g0282 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-5687C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101309999 | |||||||
| chr3:101310067 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG02559.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-5755G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310067 | |||||||
| chr3:101310095 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.335-5783C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310095 | |||||||
| chr3:101310305 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.335-5993A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310305 | |||||||
| chr3:101310377 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.335-6065G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310377 | |||||||
| chr3:101310393 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.335-6081G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310393 | |||||||
| chr3:101310415 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.335-6103G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310415 | |||||||
| chr3:101310429 | C | T | 2 | a0001c0001t0033g0052 a0001c0001t0033g0158 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.335-6117G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310429 | |||||||
| chr3:101310527 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.335-6215G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310527 | |||||||
| chr3:101310559 | C | CA | 10 | a0001c0001t0001g0281 a0001c0001t0026g0304 a0001c0001t0026g0305 others(7): Show |
11 | HG01175.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.335-6248dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | |||||||
| chr3:101310559 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0016g0211 a0001c0001t0061g0153 |
2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.335-6262_335-6248d others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | |||||||
| chr3:101310559 | CAAAAAAA others(9): Show |
C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.335-6263_335-6248d others(18): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | |||||||
| chr3:101310559 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.335-6264_335-6248d others(19): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310559 | |||||||
| chr3:101310563 | A | C | 53 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.335-6251T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310563 | |||||||
| chr3:101310577 | AAAAAAAA others(6): Show |
A | 5 | a0002c0003t0002g0271 a0002c0003t0002g0272 a0002c0003t0003g0270 others(2): Show |
5 | HG00673.hp1 HG02015.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.335-6278_335-6266d others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310577 | |||||||
| chr3:101310578 | AAAAAAAA others(5): Show |
A | 47 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(44): Show |
54 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.335-6278_335-6267d others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310578 | |||||||
| chr3:101310579 | AAAAAAAA others(4): Show |
A | 1 | a0002c0003t0002g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.335-6278_335-6268d others(13): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310579 | |||||||
| chr3:101310686 | T | C | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335-6374A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310686 | |||||||
| chr3:101310748 | A | G | 2 | a0002c0003t0002g0228 a0002c0003t0003g0024 |
3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.335-6436T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310748 | |||||||
| chr3:101310767 | T | C | 1 | a0001c0001t0065g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.335-6455A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310767 | |||||||
| chr3:101310790 | T | C | 1 | a0002c0002t0017g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.335-6478A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310790 | |||||||
| chr3:101310873 | T | C | 1 | a0002c0003t0002g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.335-6561A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101310873 | |||||||
| chr3:101311179 | T | TA | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.335-6868dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311179 | |||||||
| chr3:101311566 | G | A | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.335-7254C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311566 | |||||||
| chr3:101311714 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.335-7402T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311714 | |||||||
| chr3:101311807 | T | G | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.335-7495A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311807 | |||||||
| chr3:101311956 | C | T | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.334+7628G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101311956 | |||||||
| chr3:101312025 | C | CA | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
101 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.334+7558dupT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312025 | |||||||
| chr3:101312025 | CA | C | 52 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(49): Show |
59 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.334+7558delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312025 | |||||||
| chr3:101312036 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.334+7548G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312036 | |||||||
| chr3:101312154 | C | G | 2 | a0001c0001t0051g0226 a0001c0001t0052g0225 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.334+7430G>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312154 | |||||||
| chr3:101312333 | A | T | 1 | a0002c0003t0003g0232 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.334+7251T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312333 | |||||||
| chr3:101312507 | A | T | 1 | a0002c0003t0002g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.334+7077T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312507 | |||||||
| chr3:101312520 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.334+7064T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312520 | |||||||
| chr3:101312691 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.334+6893A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312691 | |||||||
| chr3:101312731 | A | G | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.334+6853T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312731 | |||||||
| chr3:101312972 | GGTCACAT others(10): Show |
G | 1 | a0001c0001t0014g0215 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.334+6595_334+6611d others(19): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101312972 | |||||||
| chr3:101313296 | T | C | 1 | a0001c0001t0020g0213 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.334+6288A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313296 | |||||||
| chr3:101313440 | A | G | 53 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.334+6144T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313440 | |||||||
| chr3:101313607 | C | T | 1 | a0001c0001t0026g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.334+5977G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313607 | |||||||
| chr3:101313687 | A | G | 1 | a0001c0001t0071g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.334+5897T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313687 | |||||||
| chr3:101313831 | A | G | 1 | a0001c0001t0055g0049 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.334+5753T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313831 | |||||||
| chr3:101313982 | A | G | 1 | a0002c0002t0011g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.334+5602T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101313982 | |||||||
| chr3:101314112 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+5472T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314112 | |||||||
| chr3:101314292 | T | C | 2 | a0001c0001t0013g0040 a0001c0001t0014g0039 |
2 | NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.334+5292A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314292 | |||||||
| chr3:101314433 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.334+5151G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314433 | |||||||
| chr3:101314514 | G | A | 1 | a0001c0001t0008g0022 | 2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.334+5070C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314514 | |||||||
| chr3:101314690 | T | C | 1 | a0002c0003t0005g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.334+4894A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314690 | |||||||
| chr3:101314841 | A | T | 1 | a0001c0001t0035g0036 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.334+4743T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314841 | |||||||
| chr3:101314989 | G | A | 1 | a0001c0001t0012g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.334+4595C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101314989 | |||||||
| chr3:101315250 | T | C | 67 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0010g0234 others(64): Show |
75 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.334+4334A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315250 | |||||||
| chr3:101315356 | T | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.334+4228A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315356 | |||||||
| chr3:101315517 | TA | T | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.334+4066delT | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315517 | |||||||
| chr3:101315551 | C | T | 1 | a0001c0001t0026g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.334+4033G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315551 | |||||||
| chr3:101315552 | G | A | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.334+4032C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315552 | |||||||
| chr3:101315660 | G | A | 1 | a0001c0001t0014g0215 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.334+3924C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315660 | |||||||
| chr3:101315777 | A | C | 1 | a0002c0002t0091g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334+3807T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315777 | |||||||
| chr3:101315784 | A | G | 63 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0010g0234 others(60): Show |
71 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.334+3800T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315784 | |||||||
| chr3:101315862 | C | A | 1 | a0002c0003t0097g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.334+3722G>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315862 | |||||||
| chr3:101315900 | G | GGTAAA | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3683_334+3684i others(7): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315900 | |||||||
| chr3:101315903 | A | AAGCT | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3680_334+3681i others(6): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315903 | |||||||
| chr3:101315908 | G | T | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3676C>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315908 | |||||||
| chr3:101315911 | A | ATTT | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3672_334+3673i others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315911 | |||||||
| chr3:101315912 | C | T | 3 | a0002c0002t0004g0289 a0002c0002t0015g0290 a0002c0002t0102g0288 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+3672G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315912 | |||||||
| chr3:101315958 | G | A | 1 | a0002c0002t0087g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.334+3626C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101315958 | |||||||
| chr3:101316214 | A | G | 53 | a0001c0001t0010g0234 a0002c0003t0002g0008 a0002c0003t0002g0027 others(50): Show |
60 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.334+3370T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316214 | |||||||
| chr3:101316258 | G | C | 5 | a0001c0001t0008g0217 a0001c0001t0010g0035 a0001c0001t0010g0218 others(2): Show |
6 | HG01123.hp1 HG01943.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+3326C>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316258 | |||||||
| chr3:101316302 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+3282G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316302 | |||||||
| chr3:101316455 | A | T | 1 | a0003c0004t0047g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.334+3129T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316455 | |||||||
| chr3:101316566 | T | C | 1 | a0001c0001t0063g0219 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.334+3018A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316566 | |||||||
| chr3:101316767 | A | G | 2 | a0002c0003t0058g0229 a0003c0009t0050g0230 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.334+2817T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316767 | |||||||
| chr3:101316866 | T | C | 1 | a0002c0002t0004g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.334+2718A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316866 | |||||||
| chr3:101316946 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.334+2638C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316946 | |||||||
| chr3:101316972 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+2612C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101316972 | |||||||
| chr3:101317095 | GTGGGCAT others(6): Show |
G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+2476_334+2488d others(15): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317095 | |||||||
| chr3:101317173 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+2411T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317173 | |||||||
| chr3:101317185 | G | A | 18 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0026g0304 others(15): Show |
19 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.334+2399C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317185 | |||||||
| chr3:101317937 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+1647G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101317937 | |||||||
| chr3:101318114 | C | T | 2 | a0002c0003t0002g0228 a0002c0003t0003g0024 |
3 | HG02698.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.334+1470G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318114 | |||||||
| chr3:101318148 | TAAATAAT others(4): Show |
T | 1 | a0002c0002t0009g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.334+1425_334+1435d others(13): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318148 | |||||||
| chr3:101318149 | A | AAAT | 54 | a0001c0001t0001g0007 a0001c0001t0006g0033 a0001c0001t0006g0098 others(51): Show |
57 | HG00438.hp2 HG00621.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.334+1432_334+1434d others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | A | AAATAAT | 17 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0008g0004 others(14): Show |
19 | HG00642.hp1 HG01167.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.334+1429_334+1434d others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | A | AAATAATA others(2): Show |
6 | a0001c0001t0013g0123 a0001c0001t0021g0104 a0001c0001t0037g0284 others(3): Show |
6 | HG00280.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+1426_334+1434d others(11): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | A | AAATAATA others(5): Show |
1 | a0001c0001t0013g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.334+1423_334+1434d others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | AAAT | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0163 others(15): Show |
25 | HG00597.hp1 HG00673.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.334+1432_334+1434d others(5): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | AAATAAT | A | 11 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0010g0234 others(8): Show |
12 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.334+1429_334+1434d others(8): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | AAATAATA others(2): Show |
A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.334+1426_334+1434d others(11): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | AAATAATA others(5): Show |
A | 57 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0057 others(54): Show |
60 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.334+1423_334+1434d others(14): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | AAATAATA others(8): Show |
A | 3 | a0001c0001t0001g0160 a0001c0001t0051g0226 a0001c0001t0052g0225 |
3 | HG02486.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.334+1420_334+1434d others(17): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318149 | AAATAATA others(11): Show |
A | 1 | a0002c0003t0002g0237 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334+1417_334+1434d others(20): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318149 | |||||||
| chr3:101318156 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.334+1428T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318156 | |||||||
| chr3:101318191 | A | T | 1 | a0001c0001t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.334+1393T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318191 | |||||||
| chr3:101318217 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+1367G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318217 | |||||||
| chr3:101318245 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.334+1339G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318245 | |||||||
| chr3:101318280 | C | T | 3 | a0001c0001t0036g0041 a0001c0001t0036g0043 a0008c0015t0076g0042 |
3 | HG02572.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.334+1304G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318280 | |||||||
| chr3:101318498 | T | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.334+1086A>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318498 | |||||||
| chr3:101318707 | A | G | 5 | a0001c0001t0010g0038 a0001c0001t0013g0040 a0001c0001t0014g0039 others(2): Show |
5 | NA18957.hp2 NA18973.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+877T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318707 | |||||||
| chr3:101318857 | C | T | 2 | a0001c0001t0010g0035 a0001c0001t0014g0011 |
3 | HG03490.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.334+727G>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318857 | |||||||
| chr3:101318882 | G | A | 3 | a0001c0001t0051g0226 a0001c0001t0052g0225 a0002c0003t0097g0227 |
3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.334+702C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318882 | |||||||
| chr3:101318923 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.334+661A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101318923 | |||||||
| chr3:101319132 | T | G | 5 | a0001c0001t0026g0304 a0001c0001t0026g0305 a0001c0001t0026g0307 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+452A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319132 | |||||||
| chr3:101319253 | T | G | 5 | a0002c0002t0039g0312 a0002c0002t0084g0310 a0002c0002t0086g0311 others(2): Show |
5 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+331A>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319253 | |||||||
| chr3:101319314 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334+270T>A | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319314 | |||||||
| chr3:101319453 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.334+131C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319453 | |||||||
| chr3:101319495 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.334+89C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 2/18 | chr3 | 101319495 | |||||||
| chr3:101319969 | A | G | 3 | a0001c0001t0051g0226 a0001c0001t0052g0225 a0002c0003t0097g0227 |
3 | HG02486.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.86-137T>C | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101319969 | |||||||
| chr3:101319995 | TC | T | 3 | a0001c0001t0006g0010 a0001c0001t0006g0032 a0001c0001t0006g0033 |
4 | HG01978.hp1 HG02148.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-164delG | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101319995 | |||||||
| chr3:101320020 | T | C | 3 | a0003c0004t0046g0315 a0003c0004t0048g0313 a0003c0004t0049g0314 |
3 | HG02451.hp1 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.86-188A>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320020 | |||||||
| chr3:101320030 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0224 |
3 | HG02647.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.86-198C>T | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320030 | |||||||
| chr3:101320178 | AAGT | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.85+107_85+109delAC others(1): Show |
IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320178 | |||||||
| chr3:101320263 | A | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.85+25T>G | IMPG2 | ENSG00000081148.12 | transcript | ENST00000193391.8 | protein_coding | 1/18 | chr3 | 101320263 |